Package 70518-3868-1

Brand: phenazopyridine hydrochloride

Generic: phenazopyridine
NDC Package

Package Facts

Identity

Package NDC 70518-3868-1
Digits Only 7051838681
Product NDC 70518-3868
Product ID 70518-3868_43dee455-3f27-27eb-e063-6294a90a7ce4
Description

21 TABLET in 1 BOTTLE, PLASTIC (70518-3868-1)

Marketing

Marketing Status
Marketed Since 2024-09-15
Brand phenazopyridine hydrochloride
Generic phenazopyridine
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": "43dee455-3f27-27eb-e063-6294a90a7ce4", "openfda": {"unii": ["0EWG668W17"], "rxcui": ["1094104"], "spl_set_id": ["82dc87bb-ba27-4b86-9bc9-18492975ac9f"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BOTTLE, PLASTIC (70518-3868-1)", "package_ndc": "70518-3868-1", "marketing_start_date": "20240915"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3868-3)", "package_ndc": "70518-3868-3", "marketing_start_date": "20250307"}], "brand_name": "Phenazopyridine Hydrochloride", "product_id": "70518-3868_43dee455-3f27-27eb-e063-6294a90a7ce4", "dosage_form": "TABLET", "product_ndc": "70518-3868", "generic_name": "Phenazopyridine", "labeler_name": "REMEDYREPACK INC.", "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": "20230921", "listing_expiration_date": "20261231"}