Package 71610-549-05

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71610-549-05
Digits Only 7161054905
Product NDC 71610-549
Description

4200 TABLET in 1 BOTTLE (71610-549-05)

Marketing

Marketing Status
Marketed Since 2021-04-30
Brand hydralazine hydrochloride
Generic hydralazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "547e8073-67bc-4f54-bcc9-0fb525db6687", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905222", "905225", "905395"], "spl_set_id": ["c2638ae6-a210-490f-8389-bbed6a3229c5"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "2000 TABLET in 1 BOTTLE (71610-549-02)", "package_ndc": "71610-549-02", "marketing_start_date": "20240401"}, {"sample": false, "description": "4200 TABLET in 1 BOTTLE (71610-549-05)", "package_ndc": "71610-549-05", "marketing_start_date": "20210430"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "71610-549_547e8073-67bc-4f54-bcc9-0fb525db6687", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "71610-549", "generic_name": "Hydralazine Hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydralazine Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA205236", "marketing_category": "ANDA", "marketing_start_date": "20210304", "listing_expiration_date": "20261231"}