phenazopyridine hydrochloride

Generic: phenazopyridine hydrochloride

Labeler: westminster pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name phenazopyridine hydrochloride
Generic Name phenazopyridine hydrochloride
Labeler westminster pharmaceuticals, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phenazopyridine hydrochloride 100 mg/1

Manufacturer
Westminster Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 69367-611
Product ID 69367-611_6f4d2d9d-4389-4d76-9f5e-e004d7b09a49
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2023-10-19

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69367611
Hyphenated Format 69367-611

Supplemental Identifiers

RxCUI
1094104 1094107
UNII
0EWG668W17

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 phenazopyridine hydrochloride (source: ndc)
Generic Name phenazopyridine hydrochloride (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (69367-611-01)
source: ndc

Packages (1)

69367-611-01 100 TABLET in 1 BOTTLE (69367-611-01)

Ingredients (1)

phenazopyridine hydrochloride (100 mg/1)

Linked Drug Pages (1)

Phenazopyridine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6f4d2d9d-4389-4d76-9f5e-e004d7b09a49", "openfda": {"unii": ["0EWG668W17"], "rxcui": ["1094104", "1094107"], "spl_set_id": ["20681450-859a-45b0-825c-760cbbd95ac6"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69367-611-01)", "package_ndc": "69367-611-01", "marketing_start_date": "20231019"}], "brand_name": "Phenazopyridine Hydrochloride", "product_id": "69367-611_6f4d2d9d-4389-4d76-9f5e-e004d7b09a49", "dosage_form": "TABLET", "product_ndc": "69367-611", "generic_name": "Phenazopyridine Hydrochloride", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenazopyridine Hydrochloride", "active_ingredients": [{"name": "PHENAZOPYRIDINE HYDROCHLORIDE", "strength": "100 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20231019", "listing_expiration_date": "20261231"}