Package 63739-328-10

Brand: HydrALAZINE Hydrochloride

Generic: HydrALAZINE Hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63739-328-10
Digits Only 6373932810
Product NDC 63739-328
Product ID 63739-328_2a320d81-424b-f045-e063-6294a90ac1ac
Description

10 BLISTER PACK in 1 CASE (63739-328-10) / 10 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Discontinued 2026-02-28
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": ["ORAL"], "spl_id": "2a320d81-424b-f045-e063-6294a90ac1ac", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905395"], "spl_set_id": ["faaf3493-8318-48b3-b59c-03537880744b"], "manufacturer_name": ["McKesson Corporation dba SKY Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CASE (63739-328-10)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "63739-328-10", "marketing_end_date": "20260228", "marketing_start_date": "20200201"}], "brand_name": "HydrALAZINE Hydrochloride", "product_id": "63739-328_2a320d81-424b-f045-e063-6294a90ac1ac", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "63739-328", "generic_name": "HydrALAZINE Hydrochloride", "labeler_name": "McKesson Corporation dba SKY Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HydrALAZINE Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA200770", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20130630"}