Package 70710-1110-0

Brand: cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70710-1110-0
Digits Only 7071011100
Product NDC 70710-1110
Product ID 70710-1110_b36a8686-4b30-4b42-a673-44cc58b775c3
Description

1000 TABLET in 1 BOTTLE (70710-1110-0)

Marketing

Marketing Status
Marketed Since 2017-07-20
Brand cyproheptadine hydrochloride
Generic cyproheptadine hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b36a8686-4b30-4b42-a673-44cc58b775c3", "openfda": {"upc": ["0370710111014"], "unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["766f9b59-2c72-45ac-af09-5dd6c3e16b52"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (70710-1110-0)", "package_ndc": "70710-1110-0", "marketing_start_date": "20170720"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (70710-1110-1)", "package_ndc": "70710-1110-1", "marketing_start_date": "20170720"}], "brand_name": "CYPROHEPTADINE HYDROCHLORIDE", "product_id": "70710-1110_b36a8686-4b30-4b42-a673-44cc58b775c3", "dosage_form": "TABLET", "product_ndc": "70710-1110", "generic_name": "CYPROHEPTADINE HYDROCHLORIDE", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "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"}