glipizide

Generic: glipizide

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name glipizide
Generic Name glipizide
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

glipizide 10 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-0579
Product ID 70518-0579_47f96f6e-5091-63ae-e063-6394a90af774
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075795
Listing Expiration 2027-12-31
Marketing Start 2017-06-20

Pharmacologic Class

Established (EPC)
sulfonylurea [epc]
Chemical Structure
sulfonylurea compounds [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705180579
Hyphenated Format 70518-0579

Supplemental Identifiers

RxCUI
310488
UNII
X7WDT95N5C
NUI
N0000175608 M0020795

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name glipizide (source: ndc)
Generic Name glipizide (source: ndc)
Application Number ANDA075795 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 180 TABLET in 1 BOTTLE, PLASTIC (70518-0579-0)
  • 30 TABLET in 1 BLISTER PACK (70518-0579-1)
  • 90 TABLET in 1 BOTTLE, PLASTIC (70518-0579-2)
  • 100 TABLET in 1 BOTTLE, PLASTIC (70518-0579-3)
  • 30 TABLET in 1 BLISTER PACK (70518-0579-7)
source: ndc

Packages (5)

70518-0579-0 180 TABLET in 1 BOTTLE, PLASTIC (70518-0579-0) 70518-0579-1 30 TABLET in 1 BLISTER PACK (70518-0579-1) 70518-0579-2 90 TABLET in 1 BOTTLE, PLASTIC (70518-0579-2) 70518-0579-3 100 TABLET in 1 BOTTLE, PLASTIC (70518-0579-3) 70518-0579-7 30 TABLET in 1 BLISTER PACK (70518-0579-7)

Ingredients (1)

glipizide (10 mg/1)

Linked Drug Pages (1)

Glipizide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47f96f6e-5091-63ae-e063-6394a90af774", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "rxcui": ["310488"], "spl_set_id": ["376ce3cf-4e1b-4b5f-b3e7-cc9fc4a5aeb4"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET in 1 BOTTLE, PLASTIC (70518-0579-0)", "package_ndc": "70518-0579-0", "marketing_start_date": "20170620"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-0579-1)", "package_ndc": "70518-0579-1", "marketing_start_date": "20180425"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-0579-2)", "package_ndc": "70518-0579-2", "marketing_start_date": "20180731"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (70518-0579-3)", "package_ndc": "70518-0579-3", "marketing_start_date": "20180905"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-0579-7)", "package_ndc": "70518-0579-7", "marketing_start_date": "20230211"}], "brand_name": "Glipizide", "product_id": "70518-0579_47f96f6e-5091-63ae-e063-6394a90af774", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "70518-0579", "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": "ANDA075795", "marketing_category": "ANDA", "marketing_start_date": "20170620", "listing_expiration_date": "20271231"}