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Lansoprazole - Medication Information

Product NDC Code 70771-1132
Drug Name

Lansoprazole

Type Generic
Pharm Class Inhibition Gastric Acid Secretion [PE],
Proton Pump Inhibitor [EPC],
Proton Pump Inhibitors [MoA]
Active Ingredients
Lansoprazole 15 mg/1
Route ORAL
Dosage Form TABLET, ORALLY DISINTEGRATING
RxCUI drug identifier 351260,
351261
Application Number ANDA200816
Labeler Name Zydus Lifesciences Limited
Packages
Package NDC Code Description
70771-1132-4 10 blister pack in 1 carton (70771-1132-4) / 10 tablet, orally disintegrating in 1 blister pack
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Spl product data elements

Usually a list of ingredients in a drug product.
LANSOPRAZOLE LANSOPRAZOLE LANSOPRAZOLE LANSOPRAZOLE ANHYDROUS CITRIC ACID ASPARTAME CELLULOSE, MICROCRYSTALLINE CROSPOVIDONE (15 MPA.S AT 5%) FERRIC OXIDE RED GLYCERYL MONOSTEARATE HYDROCHLORIC ACID HYPROMELLOSES MAGNESIUM CARBONATE MAGNESIUM STEARATE MANNITOL METHACRYLIC ACID AND ETHYL ACRYLATE COPOLYMER POLYACRYLIC ACID (250000 MW) POLYETHYLENE GLYCOL, UNSPECIFIED POLYSORBATE 80 SILICON DIOXIDE SODIUM HYDROXIDE SODIUM STARCH GLYCOLATE TYPE A POTATO STARCH, CORN STRAWBERRY TALC TRIETHYL CITRATE XANTHAN GUM WHITE TO OFF-WHITE STRAWBERRY ROUND 771 LANSOPRAZOLE LANSOPRAZOLE LANSOPRAZOLE LANSOPRAZOLE ANHYDROUS CITRIC ACID ASPARTAME CELLULOSE, MICROCRYSTALLINE CROSPOVIDONE (15 MPA.S AT 5%) FERRIC OXIDE RED GLYCERYL MONOSTEARATE HYDROCHLORIC ACID HYPROMELLOSES MAGNESIUM CARBONATE MAGNESIUM STEARATE MANNITOL METHACRYLIC ACID AND ETHYL ACRYLATE COPOLYMER POLYACRYLIC ACID (250000 MW) POLYETHYLENE GLYCOL, UNSPECIFIED POLYSORBATE 80 SILICON DIOXIDE SODIUM HYDROXIDE SODIUM STARCH GLYCOLATE TYPE A POTATO STARCH, CORN STRAWBERRY TALC TRIETHYL CITRATE XANTHAN GUM WHITE TO OFF-WHITE STRAWBERRY ROUND 772

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.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 70771-1132-4 Lansoprazole Delayed-release Orally Disintegrating Tablets, 15 mg R x only 100 Tablets (10 x 10 Unit Dose) NDC 70771-1133-4 Lansoprazole Delayed-release Orally Disintegrating Tablets, 30 mg R x only 100 Tablets (10 x 10 Unit Dose) Lansoprazole delayed-release orally disintegrating tablets, 15 mg Lansoprazole delayed-release orally disintegrating tablets, 30 mg

Spl medguide

Information about the patient medication guide that accompanies the drug product. Certain drugs must be dispensed with an accompanying medication guide. This field may contain information about when to consult the medication guide and the contents of the medication guide.
SPL MEDGUIDE

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