Package 70518-2640-0

Brand: oxybutynin chloride

Generic: oxybutynin chloride
NDC Package

Package Facts

Identity

Package NDC 70518-2640-0
Digits Only 7051826400
Product NDC 70518-2640
Description

30 TABLET in 1 BLISTER PACK (70518-2640-0)

Marketing

Marketing Status
Marketed Since 2020-03-26
Brand oxybutynin chloride
Generic oxybutynin chloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4a7c6cdc-4b20-7a2a-e063-6294a90aaea2", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863664"], "spl_set_id": ["1a08a16a-f16d-4ef1-95bb-6943bcae0737"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2640-0)", "package_ndc": "70518-2640-0", "marketing_start_date": "20200326"}], "brand_name": "Oxybutynin Chloride", "product_id": "70518-2640_4a7c6cdc-4b20-7a2a-e063-6294a90aaea2", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "70518-2640", "generic_name": "Oxybutynin Chloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxybutynin Chloride", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA209335", "marketing_category": "ANDA", "marketing_start_date": "20200326", "listing_expiration_date": "20271231"}