Package 70771-1076-0

Brand: cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70771-1076-0
Digits Only 7077110760
Product NDC 70771-1076
Product ID 70771-1076_465671c3-1e82-41d6-8ce4-b524d0032b15
Description

1000 TABLET in 1 BOTTLE (70771-1076-0)

Marketing

Marketing Status
Marketed Since 2017-07-20
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": "465671c3-1e82-41d6-8ce4-b524d0032b15", "openfda": {"unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["ccd7d3b2-b0c1-4f66-8d06-d21f5cfa8c1e"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (70771-1076-0)", "package_ndc": "70771-1076-0", "marketing_start_date": "20170720"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (70771-1076-1)", "package_ndc": "70771-1076-1", "marketing_start_date": "20170720"}], "brand_name": "CYPROHEPTADINE HYDROCHLORIDE", "product_id": "70771-1076_465671c3-1e82-41d6-8ce4-b524d0032b15", "dosage_form": "TABLET", "product_ndc": "70771-1076", "generic_name": "CYPROHEPTADINE HYDROCHLORIDE", "labeler_name": "Zydus Lifesciences Limited", "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"}