Package 71205-041-78
Brand: glipizide
Generic: glipizidePackage Facts
Identity
Package NDC
71205-041-78
Digits Only
7120504178
Product NDC
71205-041
Description
180 TABLET in 1 BOTTLE (71205-041-78)
Marketing
Marketing Status
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": "b46704f4-8e65-4529-a073-e1d4a2600a12", "openfda": {"nui": ["N0000175608", "M0020795"], "upc": ["0371205041908"], "unii": ["X7WDT95N5C"], "rxcui": ["310490"], "spl_set_id": ["f280acc1-d912-4f2e-b131-440e708c7b1f"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-041-30)", "package_ndc": "71205-041-30", "marketing_start_date": "20180501"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-041-60)", "package_ndc": "71205-041-60", "marketing_start_date": "20180501"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71205-041-78)", "package_ndc": "71205-041-78", "marketing_start_date": "20200813"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-041-90)", "package_ndc": "71205-041-90", "marketing_start_date": "20180501"}], "brand_name": "Glipizide", "product_id": "71205-041_b46704f4-8e65-4529-a073-e1d4a2600a12", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "71205-041", "generic_name": "Glipizide", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "5 mg/1"}], "application_number": "ANDA075795", "marketing_category": "ANDA", "marketing_start_date": "20020925", "listing_expiration_date": "20261231"}