Package 63029-105-12

Brand: uristat ultra

Generic: phenazopyridine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63029-105-12
Digits Only 6302910512
Product NDC 63029-105
Description

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

Marketing

Marketing Status
Marketed Since 2018-02-15
Brand uristat ultra
Generic phenazopyridine hydrochloride
Sample Package No

Linked Drug Pages (1)

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"}