Package 70518-2246-0

Brand: irbesartan

Generic: irbesartan
NDC Package

Package Facts

Identity

Package NDC 70518-2246-0
Digits Only 7051822460
Product NDC 70518-2246
Description

90 TABLET in 1 BOTTLE, PLASTIC (70518-2246-0)

Marketing

Marketing Status
Marketed Since 2019-08-01
Brand irbesartan
Generic irbesartan
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "49eef8a6-b5da-9999-e063-6394a90a260a", "openfda": {"nui": ["N0000000070", "N0000175561"], "unii": ["J0E2756Z7N"], "rxcui": ["200096"], "spl_set_id": ["bb58acb0-2dc0-45ee-86bb-b405b1b75cff"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-2246-0)", "package_ndc": "70518-2246-0", "marketing_start_date": "20190801"}], "brand_name": "Irbesartan", "product_id": "70518-2246_49eef8a6-b5da-9999-e063-6394a90a260a", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "70518-2246", "generic_name": "Irbesartan", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Irbesartan", "active_ingredients": [{"name": "IRBESARTAN", "strength": "300 mg/1"}], "application_number": "ANDA202910", "marketing_category": "ANDA", "marketing_start_date": "20190801", "listing_expiration_date": "20271231"}