Package 71335-1107-2

Brand: cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-1107-2
Digits Only 7133511072
Product NDC 71335-1107
Description

60 TABLET in 1 BOTTLE (71335-1107-2)

Marketing

Marketing Status
Marketed Since 2019-02-21
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": "9a366fac-a3ee-4ed0-926a-03f50fe853d5", "openfda": {"unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["ab58d4df-69d4-43ac-ac6c-871fcc6c946d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1107-1)", "package_ndc": "71335-1107-1", "marketing_start_date": "20190221"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1107-2)", "package_ndc": "71335-1107-2", "marketing_start_date": "20190221"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-1107-3)", "package_ndc": "71335-1107-3", "marketing_start_date": "20190221"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-1107-4)", "package_ndc": "71335-1107-4", "marketing_start_date": "20190221"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1107-5)", "package_ndc": "71335-1107-5", "marketing_start_date": "20190221"}], "brand_name": "CYPROHEPTADINE HYDROCHLORIDE", "product_id": "71335-1107_9a366fac-a3ee-4ed0-926a-03f50fe853d5", "dosage_form": "TABLET", "product_ndc": "71335-1107", "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": "ANDA209172", "marketing_category": "ANDA", "marketing_start_date": "20180411", "listing_expiration_date": "20261231"}