Package 42708-177-21

Brand: cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride
NDC Package Sample

Package Facts

Identity

Package NDC 42708-177-21
Digits Only 4270817721
Product NDC 42708-177
Product ID 42708-177_459ba568-5598-4ba9-e063-6394a90a0680
Description

21 TABLET in 1 BOTTLE, PLASTIC (42708-177-21)

Marketing

Marketing Status
Marketed Since 2023-06-05
Brand cyproheptadine hydrochloride
Generic cyproheptadine hydrochloride
Sample Package Yes

Linked Drug Pages (1)

Cyproheptadine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "459ba568-5598-4ba9-e063-6394a90a0680", "openfda": {"unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["fc75bd79-63b7-6388-e053-6394a90ac377"], "manufacturer_name": ["QPharma Inc"]}, "finished": true, "packaging": [{"sample": true, "description": "21 TABLET in 1 BOTTLE, PLASTIC (42708-177-21)", "package_ndc": "42708-177-21", "marketing_start_date": "20230605"}], "brand_name": "Cyproheptadine Hydrochloride", "product_id": "42708-177_459ba568-5598-4ba9-e063-6394a90a0680", "dosage_form": "TABLET", "product_ndc": "42708-177", "generic_name": "Cyproheptadine Hydrochloride", "labeler_name": "QPharma Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyproheptadine Hydrochloride", "active_ingredients": [{"name": "CYPROHEPTADINE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA206553", "marketing_category": "ANDA", "marketing_start_date": "20170117", "listing_expiration_date": "20261231"}