Package 50111-328-03

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50111-328-03
Digits Only 5011132803
Product NDC 50111-328
Product ID 50111-328_faf6c313-03e6-4bf8-ac9f-65642ae10097
Description

1000 TABLET in 1 BOTTLE (50111-328-03)

Marketing

Marketing Status
Marketed Since 1990-09-30
Brand hydralazine hydrochloride
Generic hydralazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Hydralazine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "faf6c313-03e6-4bf8-ac9f-65642ae10097", "openfda": {"upc": ["0350111327016", "0350111398016", "0350111328013"], "unii": ["FD171B778Y"], "rxcui": ["905199", "905222", "905225", "905395"], "spl_set_id": ["ddbbdb09-3202-42d7-bbb0-08331dde2f54"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (50111-328-01)", "package_ndc": "50111-328-01", "marketing_start_date": "19900930"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (50111-328-03)", "package_ndc": "50111-328-03", "marketing_start_date": "19900930"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "50111-328_faf6c313-03e6-4bf8-ac9f-65642ae10097", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "50111-328", "generic_name": "Hydralazine Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydralazine Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA088468", "marketing_category": "ANDA", "marketing_start_date": "19900930", "listing_expiration_date": "20261231"}