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Tretinoin

NDC 16714-249 · NORTHSTAR RX LLC

Generic nametretinoin
Dosage formCREAM
RouteTOPICAL
Active ingredient(s)TRETINOIN
Strength.5 mg/g
Pharmacologic classRetinoid [EPC], Retinoids [CS]
Marketing categoryANDA

Packages

16714-249-01 — 1 TUBE in 1 CARTON (16714-249-01) / 20 g in 1 TUBE

16714-249-02 — 1 TUBE in 1 CARTON (16714-249-02) / 45 g in 1 TUBE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0472-0117 — Tretinoin, 0472-1790 — Clindamycin Phosphate and Tretinoin, 0574-2201 — tretinoin, 0574-2205 — tretinoin, 0574-2225 — tretinoin, 0574-2301 — tretinoin, 0574-2325 — tretinoin, 0904-6867 — Tretinoin, 10370-268 — Tretinoin, 13548-070 — Tretinoin, 16714-250 — Tretinoin, 16714-270 — tretinoin, 21922-042 — Tretinoin, 21922-043 — Tretinoin, 21922-050 — Clindamycin Phosphate and Tretinoin Gel 1.2%/0.025%, 21922-056 — Tretinoin, 21922-057 — Tretinoin, 21922-077 — Tretinoin, 21922-078 — Tretinoin, 21922-079 — Tretinoin, +70 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.