phenazopyridine hydrochloride

Generic: phenazopyridine

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

Drug Facts

Product Profile

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

phenazopyridine hydrochloride 200 mg/1

Manufacturer
Amneal Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 65162-682
Product ID 65162-682_9b599d15-523d-4e57-a844-800d995d35e5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2011-02-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65162682
Hyphenated Format 65162-682

Supplemental Identifiers

RxCUI
1094104 1094107
UPC
0365162682106 0365162681109
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 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (65162-682-10)
source: ndc

Packages (1)

65162-682-10 100 TABLET in 1 BOTTLE (65162-682-10)

Ingredients (1)

phenazopyridine hydrochloride (200 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": "9b599d15-523d-4e57-a844-800d995d35e5", "openfda": {"upc": ["0365162682106", "0365162681109"], "unii": ["0EWG668W17"], "rxcui": ["1094104", "1094107"], "spl_set_id": ["b424b50f-990b-4018-a815-0311693cabb3"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (65162-682-10)", "package_ndc": "65162-682-10", "marketing_start_date": "20110201"}], "brand_name": "Phenazopyridine Hydrochloride", "product_id": "65162-682_9b599d15-523d-4e57-a844-800d995d35e5", "dosage_form": "TABLET", "product_ndc": "65162-682", "generic_name": "Phenazopyridine", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenazopyridine Hydrochloride", "active_ingredients": [{"name": "PHENAZOPYRIDINE HYDROCHLORIDE", "strength": "200 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20110201", "listing_expiration_date": "20261231"}