phenazopyridine hydrochloride

Generic: phenazopyridine

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name phenazopyridine hydrochloride
Generic Name phenazopyridine
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phenazopyridine hydrochloride 200 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3868
Product ID 70518-3868_43dee455-3f27-27eb-e063-6294a90a7ce4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2023-09-21

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183868
Hyphenated Format 70518-3868

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
  • 21 TABLET in 1 BOTTLE, PLASTIC (70518-3868-1)
  • 30 TABLET in 1 BLISTER PACK (70518-3868-3)
source: ndc

Packages (2)

Ingredients (1)

phenazopyridine hydrochloride (200 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "43dee455-3f27-27eb-e063-6294a90a7ce4", "openfda": {"unii": ["0EWG668W17"], "rxcui": ["1094104"], "spl_set_id": ["82dc87bb-ba27-4b86-9bc9-18492975ac9f"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BOTTLE, PLASTIC (70518-3868-1)", "package_ndc": "70518-3868-1", "marketing_start_date": "20240915"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3868-3)", "package_ndc": "70518-3868-3", "marketing_start_date": "20250307"}], "brand_name": "Phenazopyridine Hydrochloride", "product_id": "70518-3868_43dee455-3f27-27eb-e063-6294a90a7ce4", "dosage_form": "TABLET", "product_ndc": "70518-3868", "generic_name": "Phenazopyridine", "labeler_name": "REMEDYREPACK INC.", "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": "20230921", "listing_expiration_date": "20261231"}