NDC 68382-005 – Topiramate

Topiramate 25 mg/1 · Capsule, Coated Pellets · Oral

Human Prescription Drug

Product NDC68382-005

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Capsule, Coated Pellets
Route
Oral
Marketing category
ANDA · ANDA078877
Marketed since
October 14, 2009
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (6)

Package NDCDescriptionSince
68382-005-01100 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-005-01)Oct 14, 2009
68382-005-05500 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-005-05)Oct 14, 2009
68382-005-101000 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-005-10)Oct 14, 2009
68382-005-1460 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-005-14)Oct 14, 2009
68382-005-1690 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-005-16)Oct 14, 2009
68382-005-1728 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-005-17)Oct 14, 2009

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