glipizide

Generic: glipizide

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name glipizide
Generic Name glipizide
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

glipizide 10 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-701
Product ID 60687-701_237f3963-47ee-7dfa-e063-6394a90a6a1e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075795
Listing Expiration 2026-12-31
Marketing Start 2023-06-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687701
Hyphenated Format 60687-701

Supplemental Identifiers

RxCUI
310488 310490
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
  • 100 BLISTER PACK in 1 CARTON (60687-701-01) / 1 TABLET in 1 BLISTER PACK (60687-701-11)
source: ndc

Packages (1)

60687-701-01 100 BLISTER PACK in 1 CARTON (60687-701-01) / 1 TABLET in 1 BLISTER PACK (60687-701-11)

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": "237f3963-47ee-7dfa-e063-6394a90a6a1e", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "rxcui": ["310488", "310490"], "spl_set_id": ["ff6805bb-b5f0-46d3-bf1d-3333b63ff1ae"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-701-01)  / 1 TABLET in 1 BLISTER PACK (60687-701-11)", "package_ndc": "60687-701-01", "marketing_start_date": "20230601"}], "brand_name": "Glipizide", "product_id": "60687-701_237f3963-47ee-7dfa-e063-6394a90a6a1e", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "60687-701", "generic_name": "Glipizide", "labeler_name": "American Health Packaging", "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": "20230601", "listing_expiration_date": "20261231"}