uristat ultra

Generic: phenazopyridine hydrochloride

Labeler: medtech products inc.
NDC Directory HUMAN OTC DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name uristat ultra
Generic Name phenazopyridine hydrochloride
Labeler medtech products inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phenazopyridine hydrochloride 99.5 mg/1

Manufacturer
Medtech Products Inc.

Identifiers & Regulatory

Product NDC 63029-105
Product ID 63029-105_14db261b-912d-4675-b681-4162d783ae1d
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2018-02-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63029105
Hyphenated Format 63029-105

Supplemental Identifiers

RxCUI
1094147 2000033
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 uristat ultra (source: ndc)
Generic Name phenazopyridine hydrochloride (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 99.5 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (63029-105-12) / 12 TABLET in 1 BLISTER PACK
  • 3 BLISTER PACK in 1 CARTON (63029-105-30) / 10 TABLET in 1 BLISTER PACK
source: ndc

Packages (2)

63029-105-12 1 BLISTER PACK in 1 CARTON (63029-105-12) / 12 TABLET in 1 BLISTER PACK 63029-105-30 3 BLISTER PACK in 1 CARTON (63029-105-30) / 10 TABLET in 1 BLISTER PACK

Ingredients (1)

phenazopyridine hydrochloride (99.5 mg/1)

Linked Drug Pages (1)

Uristat Ultra ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "14db261b-912d-4675-b681-4162d783ae1d", "openfda": {"unii": ["0EWG668W17"], "rxcui": ["1094147", "2000033"], "spl_set_id": ["c705185f-4908-451e-993b-b0b8a73f0392"], "manufacturer_name": ["Medtech Products Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (63029-105-12)  / 12 TABLET in 1 BLISTER PACK", "package_ndc": "63029-105-12", "marketing_start_date": "20180215"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (63029-105-30)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "63029-105-30", "marketing_start_date": "20180215"}], "brand_name": "Uristat Ultra", "product_id": "63029-105_14db261b-912d-4675-b681-4162d783ae1d", "dosage_form": "TABLET", "product_ndc": "63029-105", "generic_name": "Phenazopyridine Hydrochloride", "labeler_name": "Medtech Products Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Uristat Ultra", "active_ingredients": [{"name": "PHENAZOPYRIDINE HYDROCHLORIDE", "strength": "99.5 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20180215", "listing_expiration_date": "20261231"}