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Cyproheptadine Hydrochloride

NDC 52817-210 · TRUPHARMA, LLC

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

Packages

52817-210-10 — 100 TABLET in 1 BOTTLE, PLASTIC (52817-210-10)

52817-210-50 — 500 TABLET in 1 BOTTLE, PLASTIC (52817-210-50)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

17856-0504 — Cyproheptadine Hydrochloride, 17856-1185 — CYPROHEPTADINE HYDROCHLORIDE, 27808-099 — Cyproheptadine Hydrochloride, 42708-177 — Cyproheptadine Hydrochloride, 42708-187 — CYPROHEPTADINE HYDROCHLORIDE, 50090-5491 — Cyproheptadine Hydrochloride, 50090-6129 — CYPROHEPTADINE HYDROCHLORIDE, 50268-201 — Cyproheptadine Hydrochloride, 50742-190 — CYPROHEPTADINE HYDROCHLORIDE, 51407-272 — 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, 70752-101 — CYPROHEPTADINE HYDROCHLORIDE, 70752-107 — 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.