Package 42708-187-21

Brand: cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride
NDC Package Sample

Package Facts

Identity

Package NDC 42708-187-21
Digits Only 4270818721
Product NDC 42708-187
Product ID 42708-187_45870b44-8f41-56a7-e063-6394a90a6ecf
Description

21 TABLET in 1 BOTTLE, PLASTIC (42708-187-21)

Marketing

Marketing Status
Marketed Since 2024-07-26
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": "45870b44-8f41-56a7-e063-6394a90a6ecf", "openfda": {"unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["1dfe4478-76d9-9b8f-e063-6394a90aefe8"], "manufacturer_name": ["QPharma Inc"]}, "finished": true, "packaging": [{"sample": true, "description": "21 TABLET in 1 BOTTLE, PLASTIC (42708-187-21)", "package_ndc": "42708-187-21", "marketing_start_date": "20240726"}], "brand_name": "CYPROHEPTADINE HYDROCHLORIDE", "product_id": "42708-187_45870b44-8f41-56a7-e063-6394a90a6ecf", "dosage_form": "TABLET", "product_ndc": "42708-187", "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": "ANDA212491", "marketing_category": "ANDA", "marketing_start_date": "20210224", "listing_expiration_date": "20261231"}