Package 76385-130-10

Brand: cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 76385-130-10
Digits Only 7638513010
Product NDC 76385-130
Description

1000 TABLET in 1 BOTTLE (76385-130-10)

Marketing

Marketing Status
Marketed Since 2020-03-01
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": "d68a0f7b-98e1-4d8c-a236-9d701e4e68d5", "openfda": {"unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["99fb821a-fe33-4468-9026-9729a8deff08"], "manufacturer_name": ["UNICHEM PHARMACEUTICALS (USA), INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (76385-130-01)", "package_ndc": "76385-130-01", "marketing_start_date": "20200301"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (76385-130-10)", "package_ndc": "76385-130-10", "marketing_start_date": "20200301"}], "brand_name": "Cyproheptadine Hydrochloride", "product_id": "76385-130_d68a0f7b-98e1-4d8c-a236-9d701e4e68d5", "dosage_form": "TABLET", "product_ndc": "76385-130", "generic_name": "Cyproheptadine Hydrochloride", "labeler_name": "UNICHEM PHARMACEUTICALS (USA), INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyproheptadine Hydrochloride", "active_ingredients": [{"name": "CYPROHEPTADINE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA206676", "marketing_category": "ANDA", "marketing_start_date": "20200301", "listing_expiration_date": "20271231"}