Package 50090-6129-1

Brand: cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6129-1
Digits Only 5009061291
Product NDC 50090-6129
Product ID 50090-6129_65894e51-4a95-421d-96e2-68483b3af453
Description

30 TABLET in 1 BOTTLE (50090-6129-1)

Marketing

Marketing Status
Marketed Since 2022-10-03
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": "65894e51-4a95-421d-96e2-68483b3af453", "openfda": {"unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["0e43e99b-2e0b-4f55-b93a-a6908634880d"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-6129-1)", "package_ndc": "50090-6129-1", "marketing_start_date": "20221003"}], "brand_name": "CYPROHEPTADINE HYDROCHLORIDE", "product_id": "50090-6129_65894e51-4a95-421d-96e2-68483b3af453", "dosage_form": "TABLET", "product_ndc": "50090-6129", "generic_name": "CYPROHEPTADINE HYDROCHLORIDE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYPROHEPTADINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYPROHEPTADINE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA208938", "marketing_category": "ANDA", "marketing_start_date": "20170720", "listing_expiration_date": "20261231"}