phenazopyridine hydrochloride
Generic: phenazopyridine
Labeler: northwind health company, llcDrug Facts
Product Profile
Brand Name
phenazopyridine hydrochloride
Generic Name
phenazopyridine
Labeler
northwind health company, llc
Dosage Form
TABLET
Routes
Active Ingredients
phenazopyridine hydrochloride 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
51655-424
Product ID
51655-424_48ff21cd-c20e-07ba-e063-6394a90aa36a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
UNAPPROVED DRUG OTHER
Listing Expiration
2027-12-31
Marketing Start
2022-09-22
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51655424
Hyphenated Format
51655-424
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 12 TABLET in 1 BOTTLE, PLASTIC (51655-424-27)
- 10 TABLET in 1 BOTTLE, PLASTIC (51655-424-53)
- 6 TABLET in 1 BOTTLE, PLASTIC (51655-424-87)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48ff21cd-c20e-07ba-e063-6394a90aa36a", "openfda": {"unii": ["0EWG668W17"], "rxcui": ["1094104"], "spl_set_id": ["f2f3e29f-9553-f7c3-e053-2995a90aff36"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET in 1 BOTTLE, PLASTIC (51655-424-27)", "package_ndc": "51655-424-27", "marketing_start_date": "20221219"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (51655-424-53)", "package_ndc": "51655-424-53", "marketing_start_date": "20220922"}, {"sample": false, "description": "6 TABLET in 1 BOTTLE, PLASTIC (51655-424-87)", "package_ndc": "51655-424-87", "marketing_start_date": "20220922"}], "brand_name": "Phenazopyridine Hydrochloride", "product_id": "51655-424_48ff21cd-c20e-07ba-e063-6394a90aa36a", "dosage_form": "TABLET", "product_ndc": "51655-424", "generic_name": "Phenazopyridine", "labeler_name": "Northwind Health Company, 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": "20220922", "listing_expiration_date": "20271231"}