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Bimatoprost

NDC 0781-6206 · Sandoz Inc

Generic nameBimatoprost
Dosage formSOLUTION/ DROPS
RouteOPHTHALMIC
Active ingredient(s)BIMATOPROST
Strength.3 mg/mL
Pharmacologic classProstaglandin Analog [EPC], Prostaglandins [CS]
Marketing categoryANDA

Packages

0781-6206-75 — 1 BOTTLE, WITH APPLICATOR in 1 CARTON (0781-6206-75) / 5 mL in 1 BOTTLE, WITH APPLICATOR

0781-6206-93 — 1 BOTTLE, WITH APPLICATOR in 1 CARTON (0781-6206-93) / 3 mL in 1 BOTTLE, WITH APPLICATOR

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0023-3205 — bimatoprost, 0023-3616 — bimatoprost, 0023-9652 — bimatoprost, 42571-128 — BIMATOPROST, 46708-507 — Bimatoprost, 46708-511 — bimatoprost, 60219-2149 — Bimatoprost, 60505-0583 — Bimatoprost, 62332-507 — Bimatoprost, 62332-511 — bimatoprost, 65862-802 — Bimatoprost, 68071-3590 — Bimatoprost, 68071-3612 — BIMATOPROST, 68083-295 — Bimatoprost, 68083-296 — Bimatoprost, 68083-439 — Bimatoprost, 70069-401 — Bimatoprost, 70069-402 — Bimatoprost, 70069-403 — Bimatoprost, 70756-626 — Bimatoprost, +7 more

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