NDC 68462-792 – Tretinoin

Tretinoin 10 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC68462-792

Product details

Brand name
Tretinoin
Generic name
Tretinoin
Labeler
Glenmark Pharmaceuticals Inc., USA
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA208279
Marketed since
December 23, 2016
Listing expires
December 31, 2027
Pharmacologic class
Retinoid

Active ingredients

Uses, dosage, side effects and warnings for Tretinoin →

Package NDC codes (1)

Package NDCDescriptionSince
68462-792-01100 CAPSULE in 1 BOTTLE (68462-792-01)Dec 23, 2016

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