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, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

glipizide 2.5 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-768
Product ID 60687-768_3388fa52-1c47-c130-e063-6294a90a5f28
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206928
Listing Expiration 2026-12-31
Marketing Start 2024-02-14

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687768
Hyphenated Format 60687-768

Supplemental Identifiers

RxCUI
310489 314006
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 ANDA206928 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 CARTON (60687-768-21) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-768-11)
source: ndc

Packages (1)

60687-768-21 30 BLISTER PACK in 1 CARTON (60687-768-21) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-768-11)

Ingredients (1)

glipizide (2.5 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": "3388fa52-1c47-c130-e063-6294a90a5f28", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "rxcui": ["310489", "314006"], "spl_set_id": ["aaf029d3-027e-4ae8-8ec5-3a4c16f9bd28"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (60687-768-21)  / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-768-11)", "package_ndc": "60687-768-21", "marketing_start_date": "20240214"}], "brand_name": "Glipizide", "product_id": "60687-768_3388fa52-1c47-c130-e063-6294a90a5f28", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "60687-768", "generic_name": "Glipizide", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA206928", "marketing_category": "ANDA", "marketing_start_date": "20240214", "listing_expiration_date": "20261231"}