Package 70518-3517-0

Brand: cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3517-0
Digits Only 7051835170
Product NDC 70518-3517
Product ID 70518-3517_3ab01147-5c61-b2bb-e063-6294a90a9c09
Description

30 TABLET in 1 BLISTER PACK (70518-3517-0)

Marketing

Marketing Status
Marketed Since 2022-09-13
Brand cyproheptadine hydrochloride
Generic cyproheptadine hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3ab01147-5c61-b2bb-e063-6294a90a9c09", "openfda": {"unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["7b3aed50-cc9e-4897-9735-361225e9e5f2"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3517-0)", "package_ndc": "70518-3517-0", "marketing_start_date": "20220913"}], "brand_name": "CYPROHEPTADINE HYDROCHLORIDE", "product_id": "70518-3517_3ab01147-5c61-b2bb-e063-6294a90a9c09", "dosage_form": "TABLET", "product_ndc": "70518-3517", "generic_name": "CYPROHEPTADINE HYDROCHLORIDE", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYPROHEPTADINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYPROHEPTADINE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA212491", "marketing_category": "ANDA", "marketing_start_date": "20220913", "listing_expiration_date": "20261231"}