Package 70518-3896-0

Brand: glipizide

Generic: glipizide
NDC Package

Package Facts

Identity

Package NDC 70518-3896-0
Digits Only 7051838960
Product NDC 70518-3896
Description

30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3896-0)

Marketing

Marketing Status
Marketed Since 2023-10-17
Brand glipizide
Generic glipizide
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4b91b1e5-466b-2a72-e063-6294a90a9e5c", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "rxcui": ["315107"], "spl_set_id": ["e593552f-9817-4cb5-b491-31ea57dea4b8"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3896-0)", "package_ndc": "70518-3896-0", "marketing_start_date": "20231017"}], "brand_name": "Glipizide", "product_id": "70518-3896_4b91b1e5-466b-2a72-e063-6294a90a9e5c", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "70518-3896", "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": "ANDA203499", "marketing_category": "ANDA", "marketing_start_date": "20231017", "listing_expiration_date": "20271231"}