Package 69367-611-01

Brand: phenazopyridine hydrochloride

Generic: phenazopyridine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69367-611-01
Digits Only 6936761101
Product NDC 69367-611
Product ID 69367-611_6f4d2d9d-4389-4d76-9f5e-e004d7b09a49
Description

100 TABLET in 1 BOTTLE (69367-611-01)

Marketing

Marketing Status
Marketed Since 2023-10-19
Brand phenazopyridine hydrochloride
Generic phenazopyridine hydrochloride
Sample Package No

Linked Drug Pages (1)

Phenazopyridine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6f4d2d9d-4389-4d76-9f5e-e004d7b09a49", "openfda": {"unii": ["0EWG668W17"], "rxcui": ["1094104", "1094107"], "spl_set_id": ["20681450-859a-45b0-825c-760cbbd95ac6"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69367-611-01)", "package_ndc": "69367-611-01", "marketing_start_date": "20231019"}], "brand_name": "Phenazopyridine Hydrochloride", "product_id": "69367-611_6f4d2d9d-4389-4d76-9f5e-e004d7b09a49", "dosage_form": "TABLET", "product_ndc": "69367-611", "generic_name": "Phenazopyridine Hydrochloride", "labeler_name": "Westminster Pharmaceuticals, 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": "20231019", "listing_expiration_date": "20261231"}