phenazopyridine hydrochloride

Generic: phenazopyridine hydrochloride

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name phenazopyridine hydrochloride
Generic Name phenazopyridine hydrochloride
Labeler chartwell rx, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phenazopyridine hydrochloride 200 mg/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-404
Product ID 62135-404_45ae56cd-d6c6-3ad2-e063-6394a90a8ebf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2011-08-23

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62135404
Hyphenated Format 62135-404

Supplemental Identifiers

RxCUI
1094104 1094107
UPC
0362135404604 0362135403607
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
  • 200 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (62135-404-60)
source: ndc

Packages (1)

62135-404-60 60 TABLET in 1 BOTTLE (62135-404-60)

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": "45ae56cd-d6c6-3ad2-e063-6394a90a8ebf", "openfda": {"upc": ["0362135404604", "0362135403607"], "unii": ["0EWG668W17"], "rxcui": ["1094104", "1094107"], "spl_set_id": ["9ed3cf8c-e1c1-4290-b094-25ac6f7a9a56"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (62135-404-60)", "package_ndc": "62135-404-60", "marketing_start_date": "20220901"}], "brand_name": "PHENAZOPYRIDINE HYDROCHLORIDE", "product_id": "62135-404_45ae56cd-d6c6-3ad2-e063-6394a90a8ebf", "dosage_form": "TABLET", "product_ndc": "62135-404", "generic_name": "PHENAZOPYRIDINE HYDROCHLORIDE", "labeler_name": "Chartwell RX, 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": "20110823", "listing_expiration_date": "20261231"}