NDC 68682-514 – Tretinoin

Tretinoin .4 mg/g · Gel · Topical

Human Prescription Drug

Product NDC68682-514

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
68682-514-921 TUBE in 1 CARTON (68682-514-92) / 20 g in 1 TUBEMar 14, 2013
68682-514-941 TUBE in 1 CARTON (68682-514-94) / 45 g in 1 TUBEMar 14, 2013
68682-514-951 BOTTLE, PUMP in 1 CARTON (68682-514-95) / 50 g in 1 BOTTLE, PUMPMar 14, 2013

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