Package 70518-1848-0

Brand: glipizide

Generic: glipizide
NDC Package

Package Facts

Identity

Package NDC 70518-1848-0
Digits Only 7051818480
Product NDC 70518-1848
Description

90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-1848-0)

Marketing

Marketing Status
Marketed Since 2019-02-04
Brand glipizide
Generic glipizide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "49776c86-c1df-aa95-e063-6294a90a482f", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "rxcui": ["315107"], "spl_set_id": ["03151cb5-d32b-4484-8f2a-8c5d24c7f6f1"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-1848-0)", "package_ndc": "70518-1848-0", "marketing_start_date": "20190204"}], "brand_name": "Glipizide", "product_id": "70518-1848_49776c86-c1df-aa95-e063-6294a90a482f", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "70518-1848", "generic_name": "Glipizide", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "10 mg/1"}], "application_number": "ANDA204720", "marketing_category": "ANDA", "marketing_start_date": "20190204", "listing_expiration_date": "20271231"}