NDC 82009-136 – Topiramate

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

Human Prescription Drug

Product NDC82009-136

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
Quallent Pharmaceuticals Health LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078235
Marketed since
July 24, 2023
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (1)

Package NDCDescriptionSince
82009-136-05500 TABLET, FILM COATED in 1 BOTTLE (82009-136-05)Jul 24, 2023

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