NDC 65841-648 – Topiramate

Topiramate 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC65841-648

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
Zydus Lifesciences Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078235
Marketed since
March 27, 2009
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (4)

Package NDCDescriptionSince
65841-648-01100 TABLET, FILM COATED in 1 BOTTLE (65841-648-01)Mar 27, 2009
65841-648-05500 TABLET, FILM COATED in 1 BOTTLE (65841-648-05)Mar 27, 2009
65841-648-1460 TABLET, FILM COATED in 1 BOTTLE (65841-648-14)Mar 27, 2009
65841-648-1690 TABLET, FILM COATED in 1 BOTTLE (65841-648-16)Mar 27, 2009

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