Package 51407-272-10

Brand: cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51407-272-10
Digits Only 5140727210
Product NDC 51407-272
Description

1000 TABLET in 1 BOTTLE, PLASTIC (51407-272-10)

Marketing

Marketing Status
Marketed Since 2019-08-22
Brand cyproheptadine hydrochloride
Generic cyproheptadine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3bb806b9-3446-4211-e063-6394a90aff66", "openfda": {"unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["95c03949-0e9a-e3b5-e053-2995a90a56b6"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (51407-272-10)", "package_ndc": "51407-272-10", "marketing_start_date": "20190822"}], "brand_name": "CYPROHEPTADINE HYDROCHLORIDE", "product_id": "51407-272_3bb806b9-3446-4211-e063-6394a90aff66", "dosage_form": "TABLET", "product_ndc": "51407-272", "generic_name": "CYPROHEPTADINE HYDROCHLORIDE", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYPROHEPTADINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYPROHEPTADINE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA205087", "marketing_category": "ANDA", "marketing_start_date": "20150923", "listing_expiration_date": "20261231"}