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| Product NDC Code | 25000-071 | ||||||||||||
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| Drug Name | Acetaminophen extended-release tablets, 650 mg |
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| Type | Brand | ||||||||||||
| Active Ingredients |
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| Route | ORAL | ||||||||||||
| Dosage Form | TABLET, EXTENDED RELEASE | ||||||||||||
| RxCUI drug identifier | 1148399 | ||||||||||||
| Application Number | ANDA215486 | ||||||||||||
| Labeler Name | MARKSANS PHARMA LIMITED | ||||||||||||
| Packages |
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Active ingredient
A list of the active, medicinal ingredients in the drug product.Active ingredient (in each caplet) Acetaminophen 650 mg
Dosage and administration
Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.Directions Do not take more than directed. See overdose warning adults and children 12 years and over take 2 caplets every 8 hours with water swallow whole; do not crush, chew, split, or dissolve do not take more than 6 caplets in 24 hours do not use for more than 10 days unless directed by a doctor children under 12 years ask a doctor. Other information store between 20-25°C (68-77°F) The FDA approved Dissolution methods differ from USP do not use if carton is opened. Do not use if foil inner seal is broken or missing
| adults and children 12 years and over |
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| children under 12 years |
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Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive ingredients carnauba wax, hydroxyethyl cellulose, hypromellose, magnesium stearate, microcrystalline cellulose, povidone, pregelatinized starch, sodium starch glycolate, titanium dioxide, triacetin Questions or comments ? Call at 1-877-376-4271 Mon-Fri 9.00am - 6.00pm EST
Indications and usage
A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.Uses Acetaminophen Extended-Release Tablets USP, 650 mg - Arthritis Pain temporarily relieves minor aches and pains due to: minor pain of arthritis muscular aches backache premenstrual and menstrual cramps the common cold headache toothache temporarily reduces fever. Acetaminophen Extended-Release Tablets USP, 650 mg - Muscle Aches and Pain temporarily relieves minor aches and pains due to: muscular aches backache minor pain of arthritis toothache premenstrual and menstrual cramps headache the common cold temporarily reduces fever
Purpose
Information about the drug product’s indications for use.Purpose Pain reliever/fever reducer
Spl product data elements
Usually a list of ingredients in a drug product.Acetaminophen Extended-Release Tablets, 650 mg Acetaminophen ACETAMINOPHEN ACETAMINOPHEN STARCH, CORN POVIDONE K30 MAGNESIUM STEARATE HYPROMELLOSE, UNSPECIFIED TRIACETIN CARNAUBA WAX TITANIUM DIOXIDE MICROCRYSTALLINE CELLULOSE SODIUM STARCH GLYCOLATE TYPE A HYDROXYETHYL CELLULOSE (140 MPA.S AT 5%) White to off white 71 Acetaminophen Extended-Release Tablets, 650 mg Acetaminophen ACETAMINOPHEN ACETAMINOPHEN STARCH, CORN POVIDONE K30 MAGNESIUM STEARATE HYPROMELLOSE, UNSPECIFIED TRIACETIN CARNAUBA WAX TITANIUM DIOXIDE MICROCRYSTALLINE CELLULOSE SODIUM STARCH GLYCOLATE TYPE A HYDROXYETHYL CELLULOSE (140 MPA.S AT 5%) white to off white 71
Package label principal display panel
The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.PRINCIPAL DISPLAY PANEL NDC 25000-071-02 Acetaminophen Extended-Release Tablets USP, 650 mg - Arthritis Pain 24 count carton label NDC 25000-071-02 Acetaminophen Extended-Release Tablets USP, 650 mg- Arthritis Pain 24 count bottle label NDC 25000-071-08 Acetaminophen Extended-Release Tablets USP, 650 mg- Arthritis Pain 100 count carton label NDC 25000-071-08 Acetaminophen Extended-Release Tablets USP, 650 mg- Arthritis Pain 100 count bottle label NDC 25000-071-10 Acetaminophen Extended-Release Tablets USP, 650 mg- Arthritis Pain 225 count carton label NDC 25000-071-10 Acetaminophen Extended-Release Tablets USP, 650 mg- Arthritis Pain 225 count bottle label NDC 25000-071-11 Acetaminophen Extended-Release Tablets USP, 650 mg- Arthritis Pain 290 count carton label NDC 25000-071-11 Acetaminophen Extended-Release Tablets USP, 650 mg- Arthritis Pain 290 count bottle label NDC 25000-071-45 Acetaminophen Extended-Release Tablets USP, 650 mg- Arthritis Pain 400 count bottle label NDC 25000-108-02 Acetaminophen Extended-Release Tablets USP, 650 mg - Muscle Aches and Pain 24 count carton label NDC 25000-108-02 Acetaminophen Extended-Release Tablets USP, 650 mg - Muscle Aches and Pain 24 count bottle label NDC 25000-108-08 Acetaminophen Extended-Release Tablets USP, 650 mg - Muscle Aches and Pain 100 count carton label NDC 25000-108-08 Acetaminophen Extended-Release Tablets USP, 650 mg - Muscle Aches and Pain 100 count bottle label aceta-24s-carton aceta-24s-label aceta-100s-carton aceta-100s-label aceta-225s-carton aceta-225s-label aceta-290s-carton aceta-290s-label aceta-400s-label aceta-musclepain-24s-carton aceta-musclepain-24s-label aceta-musclepain-100s-carton aceta-muscle-100s-label
Ask doctor
Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.Ask a doctor before use if you have liver disease.
Ask doctor or pharmacist
Information about when a doctor or pharmacist should be consulted about drug/drug or drug/food interactions before using a drug product.Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin.
Do not use
Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.Do not use with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist. if you are allergic to acetaminophen or any of the inactive ingredients in this product.
Keep out of reach of children
Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.Keep out of reach of children. Overdose warning: In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222). Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.
Stop use
Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.Stop use and ask a doctor if pain gets worse or lasts more than 10 days fever gets worse or lasts more than 3 days new symptoms occur redness or swelling is present These could be signs of a serious condition.
Pregnancy or breast feeding
Pregnancy or Breast feedingIf pregnant or breast-feeding ask a health professional before use.
Warnings
Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.Warnings Liver warning This product contains acetaminophen. Severe liver damage may occur if you take more than 6 caplets in 24 hours, which is the maximum daily amount with other drugs containing acetaminophen 3 or more alcoholic drinks every day while using this product. Allergy alert: acetaminophen may cause severe skin reactions. Symptoms may include: skin reddening blisters rash If a skin reaction occurs, stop use and seek medical help right away.
Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API