NDC 68084-075 – Tretinoin

Tretinoin 10 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC68084-075

Product details

Brand name
Tretinoin
Generic name
Tretinoin
Labeler
American Health Packaging
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA201687
Marketed since
July 18, 2013
Listing expires
December 31, 2026
Pharmacologic class
Retinoid

Active ingredients

Uses, dosage, side effects and warnings for Tretinoin →

Package NDC codes (1)

Package NDCDescriptionSince
68084-075-213 BLISTER PACK in 1 CARTON (68084-075-21) / 10 CAPSULE in 1 BLISTER PACK (68084-075-11)Jul 18, 2013

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