phenazopyridine hydrochloride

Generic: phenazopyridine

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name phenazopyridine hydrochloride
Generic Name phenazopyridine
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phenazopyridine hydrochloride 200 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2750
Product ID 71335-2750_47073c97-afea-4098-80fb-68d4bd2c6d00
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 713352750
Hyphenated Format 71335-2750

Supplemental Identifiers

RxCUI
1094104
UNII
0EWG668W17

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
  • 9 TABLET in 1 BOTTLE (71335-2750-1)
  • 20 TABLET in 1 BOTTLE (71335-2750-2)
  • 30 TABLET in 1 BOTTLE (71335-2750-3)
  • 10 TABLET in 1 BOTTLE (71335-2750-4)
  • 15 TABLET in 1 BOTTLE (71335-2750-5)
  • 6 TABLET in 1 BOTTLE (71335-2750-6)
  • 90 TABLET in 1 BOTTLE (71335-2750-7)
  • 12 TABLET in 1 BOTTLE (71335-2750-8)
  • 18 TABLET in 1 BOTTLE (71335-2750-9)
source: ndc

Packages (9)

71335-2750-1 9 TABLET in 1 BOTTLE (71335-2750-1) 71335-2750-2 20 TABLET in 1 BOTTLE (71335-2750-2) 71335-2750-3 30 TABLET in 1 BOTTLE (71335-2750-3) 71335-2750-4 10 TABLET in 1 BOTTLE (71335-2750-4) 71335-2750-5 15 TABLET in 1 BOTTLE (71335-2750-5) 71335-2750-6 6 TABLET in 1 BOTTLE (71335-2750-6) 71335-2750-7 90 TABLET in 1 BOTTLE (71335-2750-7) 71335-2750-8 12 TABLET in 1 BOTTLE (71335-2750-8) 71335-2750-9 18 TABLET in 1 BOTTLE (71335-2750-9)

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": "47073c97-afea-4098-80fb-68d4bd2c6d00", "openfda": {"unii": ["0EWG668W17"], "rxcui": ["1094104"], "spl_set_id": ["3c9b98b0-72a5-44c5-a4de-7e950c5176c9"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET in 1 BOTTLE (71335-2750-1)", "package_ndc": "71335-2750-1", "marketing_start_date": "20250724"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-2750-2)", "package_ndc": "71335-2750-2", "marketing_start_date": "20250724"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2750-3)", "package_ndc": "71335-2750-3", "marketing_start_date": "20250724"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-2750-4)", "package_ndc": "71335-2750-4", "marketing_start_date": "20250724"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (71335-2750-5)", "package_ndc": "71335-2750-5", "marketing_start_date": "20250724"}, {"sample": false, "description": "6 TABLET in 1 BOTTLE (71335-2750-6)", "package_ndc": "71335-2750-6", "marketing_start_date": "20250724"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2750-7)", "package_ndc": "71335-2750-7", "marketing_start_date": "20250724"}, {"sample": false, "description": "12 TABLET in 1 BOTTLE (71335-2750-8)", "package_ndc": "71335-2750-8", "marketing_start_date": "20250724"}, {"sample": false, "description": "18 TABLET in 1 BOTTLE (71335-2750-9)", "package_ndc": "71335-2750-9", "marketing_start_date": "20250724"}], "brand_name": "Phenazopyridine Hydrochloride", "product_id": "71335-2750_47073c97-afea-4098-80fb-68d4bd2c6d00", "dosage_form": "TABLET", "product_ndc": "71335-2750", "generic_name": "Phenazopyridine", "labeler_name": "Bryant Ranch Prepack", "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"}