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| Product NDC Code | 70771-1052 | ||||||||
|---|---|---|---|---|---|---|---|---|---|
| Drug Name | Modafinil |
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| Type | Generic | ||||||||
| Pharm Class | Central Nervous System Stimulation [PE], Increased Sympathetic Activity [PE], Sympathomimetic-like Agent [EPC] |
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| Active Ingredients |
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| Route | ORAL | ||||||||
| Dosage Form | TABLET | ||||||||
| RxCUI drug identifier | 205324, 260218 |
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| Application Number | ANDA209966 | ||||||||
| Labeler Name | Zydus Lifesciences Limited | ||||||||
| Packages |
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| Check if available Online | Get Medication Prices online with Discount |
Spl product data elements
Usually a list of ingredients in a drug product.Modafinil Modafinil MODAFINIL MODAFINIL CELLULOSE, MICROCRYSTALLINE CROSCARMELLOSE SODIUM LACTOSE MONOHYDRATE MAGNESIUM STEARATE POVIDONE STARCH, CORN OFF-WHITE CAPSULE 1072 Modafinil Modafinil MODAFINIL MODAFINIL CELLULOSE, MICROCRYSTALLINE CROSCARMELLOSE SODIUM LACTOSE MONOHYDRATE MAGNESIUM STEARATE POVIDONE STARCH, CORN OFF-WHITE CAPSULE 10;73
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 70771-1051-3 Modafinil Tablets USP, 100 mg 30 Tablets Rx only NDC 70771-1052-3 Modafinil Tablets USP, 200 mg 30 Tablets Rx only Modafinil Tablets USP, 100mg and 200mg Modafinil Tablets USP, 100mg and 200mg
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