Package 71335-2964-1

Brand: cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2964-1
Digits Only 7133529641
Product NDC 71335-2964
Product ID 71335-2964_ccf448d1-4daf-4db0-9134-6ea5bf0409eb
Description

90 TABLET in 1 BOTTLE (71335-2964-1)

Marketing

Marketing Status
Marketed Since 2025-11-10
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": "ccf448d1-4daf-4db0-9134-6ea5bf0409eb", "openfda": {"unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["22eaef18-b5cc-421a-910e-d569f00b4599"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2964-1)", "package_ndc": "71335-2964-1", "marketing_start_date": "20251110"}], "brand_name": "CYPROHEPTADINE HYDROCHLORIDE", "product_id": "71335-2964_ccf448d1-4daf-4db0-9134-6ea5bf0409eb", "dosage_form": "TABLET", "product_ndc": "71335-2964", "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"}