Package 62135-403-60

Brand: phenazopyridine hydrochloride

Generic: phenazopyridine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62135-403-60
Digits Only 6213540360
Product NDC 62135-403
Description

60 TABLET in 1 BOTTLE (62135-403-60)

Marketing

Marketing Status
Marketed Since 2022-09-01
Brand phenazopyridine hydrochloride
Generic phenazopyridine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45ae56cd-d6c6-3ad2-e063-6394a90a8ebf", "openfda": {"upc": ["0362135404604", "0362135403607"], "unii": ["0EWG668W17"], "rxcui": ["1094104", "1094107"], "spl_set_id": ["9ed3cf8c-e1c1-4290-b094-25ac6f7a9a56"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (62135-403-60)", "package_ndc": "62135-403-60", "marketing_start_date": "20220901"}], "brand_name": "PHENAZOPYRIDINE HYDROCHLORIDE", "product_id": "62135-403_45ae56cd-d6c6-3ad2-e063-6394a90a8ebf", "dosage_form": "TABLET", "product_ndc": "62135-403", "generic_name": "PHENAZOPYRIDINE HYDROCHLORIDE", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PHENAZOPYRIDINE HYDROCHLORIDE", "active_ingredients": [{"name": "PHENAZOPYRIDINE HYDROCHLORIDE", "strength": "100 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20110823", "listing_expiration_date": "20261231"}