Package 70710-1988-7

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70710-1988-7
Digits Only 7071019887
Product NDC 70710-1988
Product ID 70710-1988_35a2dca2-f3f1-4718-85b7-79597d6e7f43
Description

25 VIAL in 1 PACKAGE (70710-1988-7) / 1 mL in 1 VIAL (70710-1988-1)

Marketing

Marketing Status
Marketed Since 2025-04-28
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": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "35a2dca2-f3f1-4718-85b7-79597d6e7f43", "openfda": {"upc": ["0370710198817"], "unii": ["FD171B778Y"], "rxcui": ["966571"], "spl_set_id": ["f0db9c3c-d841-46f9-8409-9ffca83d7a97"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 PACKAGE (70710-1988-7)  / 1 mL in 1 VIAL (70710-1988-1)", "package_ndc": "70710-1988-7", "marketing_start_date": "20250428"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "70710-1988_35a2dca2-f3f1-4718-85b7-79597d6e7f43", "dosage_form": "INJECTION", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "70710-1988", "generic_name": "Hydralazine Hydrochloride", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydralazine Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA202938", "marketing_category": "ANDA", "marketing_start_date": "20250428", "listing_expiration_date": "20261231"}