50090-1755 : Topiramate 100 mg Oral Tablet, Film Coated

NDC:	50090-1755
Labeler:	A-s Medication Solutions
Product Type:	Human Prescription Drug
Drug Name:	Topiramate
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA077627
Rev. Date:	Mar 27, 2009

NDC Package Codes:

50090-1755-0: 60 TABLET, FILM COATED IN 1 BOTTLE (50090‑1755‑0)
50090-1755-2: 90 TABLET, FILM COATED IN 1 BOTTLE (50090‑1755‑2)

Active Ingredients:

Topiramate

Dosage Strength:

100 mg

Pharmaceutical Classes:

Decreased Central Nervous System Disorganized Electrical Activity [PE]
Cytochrome P450 3A4 Inducers [MoA]
Cytochrome P450 2C19 Inhibitors [MoA]

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.