NDC 50268-808 – Topiramate

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

Human Prescription Drug

Product NDC50268-808

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
AvPAK
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078235
Marketed since
June 8, 2026
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (1)

Package NDCDescriptionSince
50268-808-1550 BLISTER PACK in 1 BOX (50268-808-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-808-11)Jun 8, 2026

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