hydralazine hydrochloride

Generic: hydralazine hydrochloride

Labeler: modavar pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydralazine hydrochloride
Generic Name hydralazine hydrochloride
Labeler modavar pharmaceuticals llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydralazine hydrochloride 100 mg/1

Manufacturer
Modavar Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 72241-006
Product ID 72241-006_2be4a232-7aa2-44f8-ba8c-f5b64677c1b7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203845
Listing Expiration 2026-12-31
Marketing Start 2015-12-29

Pharmacologic Class

Classes
arteriolar vasodilation [pe] arteriolar vasodilator [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72241006
Hyphenated Format 72241-006

Supplemental Identifiers

RxCUI
905222 905225 905395
UPC
0372241006111
UNII
FD171B778Y

Packaging Origin

Original Packager
true

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 ANDA203845 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72241-006-05)
  • 1000 TABLET in 1 BOTTLE (72241-006-11)
source: ndc

Packages (2)

72241-006-05 100 TABLET in 1 BOTTLE (72241-006-05) 72241-006-11 1000 TABLET in 1 BOTTLE (72241-006-11)

Ingredients (1)

hydralazine hydrochloride (100 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": "2be4a232-7aa2-44f8-ba8c-f5b64677c1b7", "openfda": {"upc": ["0372241006111"], "unii": ["FD171B778Y"], "rxcui": ["905222", "905225", "905395"], "spl_set_id": ["a456bc34-0c79-44f4-9119-50028a978f5f"], "manufacturer_name": ["Modavar Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72241-006-05)", "package_ndc": "72241-006-05", "marketing_start_date": "20151229"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (72241-006-11)", "package_ndc": "72241-006-11", "marketing_start_date": "20151229"}], "brand_name": "HYDRALAZINE HYDROCHLORIDE", "product_id": "72241-006_2be4a232-7aa2-44f8-ba8c-f5b64677c1b7", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "72241-006", "generic_name": "hydralazine hydrochloride", "labeler_name": "Modavar Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDRALAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA203845", "marketing_category": "ANDA", "marketing_start_date": "20151229", "listing_expiration_date": "20261231"}