NDC 68682-513 – Tretinoin

Tretinoin 1 mg/g · Gel · Topical

Human Prescription Drug

Product NDC68682-513

Product details

Brand name
Tretinoin
Generic name
Tretinoin
Labeler
Oceanside Pharmaceuticals
Dosage form
Gel
Route
Topical
Marketing category
NDA AUTHORIZED GENERIC · NDA020475
Marketed since
March 14, 2013
Listing expires
December 31, 2027
Pharmacologic class
Retinoid

Active ingredients

Uses, dosage, side effects and warnings for Tretinoin →

Package NDC codes (3)

Package NDCDescriptionSince
68682-513-821 TUBE in 1 CARTON (68682-513-82) / 20 g in 1 TUBEMar 14, 2013
68682-513-841 TUBE in 1 CARTON (68682-513-84) / 45 g in 1 TUBEMar 14, 2013
68682-513-851 BOTTLE, PUMP in 1 CARTON (68682-513-85) / 50 g in 1 BOTTLE, PUMPMar 14, 2013

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