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PROMETHAZINE HYDROCHLORIDE

NDC 10702-004 · KVK-Tech, Inc.

Generic namepromethazine hydrochloride
Dosage formTABLET
RouteORAL
Active ingredient(s)PROMETHAZINE HYDROCHLORIDE
Strength50 mg/1
Pharmacologic classPhenothiazine [EPC], Phenothiazines [CS]
Marketing categoryANDA

Packages

10702-004-01 — 100 TABLET in 1 BOTTLE (10702-004-01)

10702-004-10 — 1000 TABLET in 1 BOTTLE (10702-004-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0641-6085 — Promethazine Hydrochloride, 0641-6208 — Promethazine Hydrochloride, 0713-0132 — promethazine hydrochloride, 0713-0526 — Promethazine Hydrochloride, 0713-0536 — promethazine hydrochloride, 0713-0780 — Promethazine Hydrochloride and Dextromethorphan Hydrobromide, 0713-0823 — Promethazine Hydrochloride and Codeine Phosphate, 0904-7304 — Promethazine Hydrochloride, 10702-002 — promethazine hydrochloride, 10702-003 — promethazine hydrochloride, 17856-0059 — promethazine hydrochloride, 17856-0065 — Promethazine Hydrochloride and Codeine Phosphate, 17856-0155 — Promethazine Hydrochloride and Dextromethorphan Hydrobromide Oral Solution, 17856-4023 — promethazine hydrochloride, 17856-4024 — Promethazine Hydrochloride and Dextromethorphan Hydrobromide, 27808-051 — promethazine hydrochloride, 27808-057 — Promethazine Hydrochloride and Dextromethorphan Hydrobromide, 27808-065 — Promethazine Hydrochloride and Codeine Phosphate, 31722-040 — Promethazine Hydrochloride, 31722-041 — Promethazine Hydrochloride, +133 more

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