NDC 63187-283 – Topiramate

Topiramate 100 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC63187-283

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077627
Marketed since
March 27, 2009
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (3)

Package NDCDescriptionSince
63187-283-3030 TABLET, FILM COATED in 1 BOTTLE (63187-283-30)Jan 1, 2019
63187-283-6060 TABLET, FILM COATED in 1 BOTTLE (63187-283-60)Jan 1, 2019
63187-283-9090 TABLET, FILM COATED in 1 BOTTLE (63187-283-90)Jan 1, 2019

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