Package 68071-5285-1

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-5285-1
Digits Only 6807152851
Product NDC 68071-5285
Product ID 68071-5285_297a3678-170d-5f0f-e063-6394a90aec48
Description

100 TABLET in 1 BOTTLE (68071-5285-1)

Marketing

Marketing Status
Marketed Since 2020-06-18
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": "297a3678-170d-5f0f-e063-6394a90aec48", "openfda": {"upc": ["0368071528510"], "unii": ["FD171B778Y"], "rxcui": ["905222"], "spl_set_id": ["a862321d-ebc1-7676-e053-2995a90a5861"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68071-5285-1)", "package_ndc": "68071-5285-1", "marketing_start_date": "20200618"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "68071-5285_297a3678-170d-5f0f-e063-6394a90aec48", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "68071-5285", "generic_name": "Hydralazine Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydralazine Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA040901", "marketing_category": "ANDA", "marketing_start_date": "20100101", "listing_expiration_date": "20261231"}