Package 16571-805-01

Brand: cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 16571-805-01
Digits Only 1657180501
Product NDC 16571-805
Product ID 16571-805_93f4f73b-1ff4-4a64-a8ec-4a574abc3dd6
Description

100 TABLET in 1 BOTTLE (16571-805-01)

Marketing

Marketing Status
Marketed Since 2022-02-10
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": "93f4f73b-1ff4-4a64-a8ec-4a574abc3dd6", "openfda": {"unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["c5e9e983-d0d2-4f87-beae-0d853ca43983"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (16571-805-01)", "package_ndc": "16571-805-01", "marketing_start_date": "20220210"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (16571-805-10)", "package_ndc": "16571-805-10", "marketing_start_date": "20220210"}], "brand_name": "Cyproheptadine Hydrochloride", "product_id": "16571-805_93f4f73b-1ff4-4a64-a8ec-4a574abc3dd6", "dosage_form": "TABLET", "product_ndc": "16571-805", "generic_name": "Cyproheptadine Hydrochloride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyproheptadine Hydrochloride", "active_ingredients": [{"name": "CYPROHEPTADINE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA207555", "marketing_category": "ANDA", "marketing_start_date": "20220209", "listing_expiration_date": "20261231"}