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CYPROHEPTADINE HYDROCHLORIDE

NDC 42708-187 · QPharma Inc

Generic nameCYPROHEPTADINE HYDROCHLORIDE
Dosage formTABLET
RouteORAL
Active ingredient(s)CYPROHEPTADINE HYDROCHLORIDE
Strength4 mg/1
Marketing categoryANDA

Packages

42708-187-21 — 21 TABLET in 1 BOTTLE, PLASTIC (42708-187-21)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0115-1757 — Cyproheptadine Hydrochloride, 16571-805 — Cyproheptadine Hydrochloride, 17856-0504 — Cyproheptadine Hydrochloride, 17856-1185 — CYPROHEPTADINE HYDROCHLORIDE, 27808-099 — Cyproheptadine Hydrochloride, 42708-177 — Cyproheptadine Hydrochloride, 50090-5491 — Cyproheptadine Hydrochloride, 50090-6129 — CYPROHEPTADINE HYDROCHLORIDE, 50268-201 — Cyproheptadine Hydrochloride, 50742-190 — CYPROHEPTADINE HYDROCHLORIDE, 51407-272 — CYPROHEPTADINE HYDROCHLORIDE, 52817-210 — Cyproheptadine Hydrochloride, 52817-415 — Cyproheptadine Hydrochloride, 62135-236 — Cyproheptadine Hydrochloride, 62135-949 — CYPROHEPTADINE HYDROCHLORIDE, 64380-795 — CYPROHEPTADINE HYDROCHLORIDE, 64980-504 — Cyproheptadine Hydrochloride, 70518-3517 — CYPROHEPTADINE HYDROCHLORIDE, 70518-4667 — Cyproheptadine Hydrochloride, 70710-1110 — CYPROHEPTADINE HYDROCHLORIDE, +13 more

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