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Griseofulvin - 0603-9171-54 - (Griseofulvin)

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Drug Information of Griseofulvin

Product NDC: 0603-9171
Proprietary Name: Griseofulvin
Non Proprietary Name: Griseofulvin
Active Ingredient(s): 125    mg/5mL & nbsp;   Griseofulvin
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Griseofulvin

Product NDC: 0603-9171
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065438
Marketing Category: ANDA
Start Marketing Date: 20101008

Package Information of Griseofulvin

Package NDC: 0603-9171-54
Package Description: 118 mL in 1 BOTTLE, PLASTIC (0603-9171-54)

NDC Information of Griseofulvin

NDC Code 0603-9171-54
Proprietary Name Griseofulvin
Package Description 118 mL in 1 BOTTLE, PLASTIC (0603-9171-54)
Product NDC 0603-9171
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Griseofulvin
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20101008
Marketing Category Name ANDA
Labeler Name Qualitest Pharmaceuticals
Substance Name GRISEOFULVIN
Strength Number 125
Strength Unit mg/5mL
Pharmaceutical Classes Decreased Mitosis [PE],Microtubule Inhibition [PE],Tubulin Inhibiting Agent [EPC]

Complete Information of Griseofulvin


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