NDC 72162-1220 – Tretinoin

Tretinoin 10 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC72162-1220

Product details

Brand name
Tretinoin
Generic name
Tretinoin
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA201687
Marketed since
October 24, 2012
Listing expires
December 31, 2026
Pharmacologic class
Retinoid

Active ingredients

Uses, dosage, side effects and warnings for Tretinoin →

Package NDC codes (2)

Package NDCDescriptionSince
72162-1220-1100 CAPSULE in 1 BOTTLE (72162-1220-1)Feb 9, 2024
72162-1220-330 CAPSULE in 1 BOTTLE (72162-1220-3)Feb 9, 2024

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