Package 50268-201-15

Brand: cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50268-201-15
Digits Only 5026820115
Product NDC 50268-201
Product ID 50268-201_426ac91c-cb7d-1fe3-e063-6394a90a1d4d
Description

50 BLISTER PACK in 1 BOX (50268-201-15) / 1 TABLET in 1 BLISTER PACK (50268-201-11)

Marketing

Marketing Status
Marketed Since 2025-10-30
Brand cyproheptadine hydrochloride
Generic cyproheptadine hydrochloride
Sample Package No

Linked Drug Pages (1)

Cyproheptadine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "426ac91c-cb7d-1fe3-e063-6394a90a1d4d", "openfda": {"unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["426acecc-aef4-099c-e063-6294a90a54eb"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-201-15)  / 1 TABLET in 1 BLISTER PACK (50268-201-11)", "package_ndc": "50268-201-15", "marketing_start_date": "20251030"}], "brand_name": "Cyproheptadine Hydrochloride", "product_id": "50268-201_426ac91c-cb7d-1fe3-e063-6394a90a1d4d", "dosage_form": "TABLET", "product_ndc": "50268-201", "generic_name": "Cyproheptadine Hydrochloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyproheptadine Hydrochloride", "active_ingredients": [{"name": "CYPROHEPTADINE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA040537", "marketing_category": "ANDA", "marketing_start_date": "20251030", "listing_expiration_date": "20261231"}