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Modafinil - Medication Information

Product NDC Code 70771-1052
Drug Name

Modafinil

Type Generic
Pharm Class Central Nervous System Stimulation [PE],
Increased Sympathetic Activity [PE],
Sympathomimetic-like Agent [EPC]
Active Ingredients
Modafinil 200 mg/1
Route ORAL
Dosage Form TABLET
RxCUI drug identifier 205324,
260218
Application Number ANDA209966
Labeler Name Zydus Lifesciences Limited
Packages
Package NDC Code Description
70771-1052-1 100 tablet in 1 bottle (70771-1052-1)
70771-1052-3 30 tablet in 1 bottle (70771-1052-3)
70771-1052-9 90 tablet in 1 bottle (70771-1052-9)
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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