HydrALAZINE Hydrochloride

Generic: HydrALAZINE Hydrochloride

Labeler: McKesson Corporation dba SKY Packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive

Drug Facts

Product Profile

Brand Name HydrALAZINE Hydrochloride
Generic Name HydrALAZINE Hydrochloride
Labeler McKesson Corporation dba SKY Packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

HYDRALAZINE HYDROCHLORIDE 50 mg/1

Identifiers & Regulatory

Product NDC 63739-328
Product ID 63739-328_2a320d81-424b-f045-e063-6294a90ac1ac
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200770
Marketing Start 2013-06-30
Marketing End 2026-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63739328
Hyphenated Format 63739-328

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name HydrALAZINE Hydrochloride (source: ndc)
Generic Name HydrALAZINE Hydrochloride (source: ndc)
Application Number ANDA200770 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 CASE (63739-328-10) / 10 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

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

Ingredients (1)

HYDRALAZINE HYDROCHLORIDE (50 mg/1)

Linked Drug Pages (1)

HydrALAZINE Hydrochloride ndc-match (0.9)

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"}