Package 71335-2453-4

Brand: cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2453-4
Digits Only 7133524534
Product NDC 71335-2453
Description

100 TABLET in 1 BOTTLE (71335-2453-4)

Marketing

Marketing Status
Marketed Since 2024-08-20
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": "eb9db456-0185-416b-a9c7-875b5694be5e", "openfda": {"unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["5d0db096-f35d-4065-bff1-2fd7ef5a1a6f"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2453-1)", "package_ndc": "71335-2453-1", "marketing_start_date": "20240820"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-2453-2)", "package_ndc": "71335-2453-2", "marketing_start_date": "20240820"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-2453-3)", "package_ndc": "71335-2453-3", "marketing_start_date": "20240820"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-2453-4)", "package_ndc": "71335-2453-4", "marketing_start_date": "20240820"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2453-5)", "package_ndc": "71335-2453-5", "marketing_start_date": "20240820"}], "brand_name": "CYPROHEPTADINE HYDROCHLORIDE", "product_id": "71335-2453_eb9db456-0185-416b-a9c7-875b5694be5e", "dosage_form": "TABLET", "product_ndc": "71335-2453", "generic_name": "CYPROHEPTADINE HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "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"}