Package 50090-5491-1

Brand: cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-5491-1
Digits Only 5009054911
Product NDC 50090-5491
Product ID 50090-5491_28b91c2a-e33a-4b09-8636-4c53ea6f1358
Description

30 TABLET in 1 BOTTLE (50090-5491-1)

Marketing

Marketing Status
Marketed Since 2021-03-16
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": "28b91c2a-e33a-4b09-8636-4c53ea6f1358", "openfda": {"unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["7e156e5e-e4cc-420b-8f1a-af123eaa9156"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-5491-1)", "package_ndc": "50090-5491-1", "marketing_start_date": "20210316"}], "brand_name": "Cyproheptadine Hydrochloride", "product_id": "50090-5491_28b91c2a-e33a-4b09-8636-4c53ea6f1358", "dosage_form": "TABLET", "product_ndc": "50090-5491", "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": "ANDA206553", "marketing_category": "ANDA", "marketing_start_date": "20170117", "listing_expiration_date": "20261231"}