glipizide

Generic: glipizide

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name glipizide
Generic Name glipizide
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

glipizide 10 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-861
Product ID 43063-861_3a212166-4cbf-fa96-e063-6394a90a5cd2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075795
Listing Expiration 2026-12-31
Marketing Start 2002-09-25

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43063861
Hyphenated Format 43063-861

Supplemental Identifiers

RxCUI
310488
UPC
0343063861301
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
  • 14 TABLET in 1 BOTTLE, PLASTIC (43063-861-14)
  • 30 TABLET in 1 BOTTLE, PLASTIC (43063-861-30)
  • 60 TABLET in 1 BOTTLE, PLASTIC (43063-861-60)
  • 90 TABLET in 1 BOTTLE, PLASTIC (43063-861-90)
  • 180 TABLET in 1 BOTTLE, PLASTIC (43063-861-93)
  • 120 TABLET in 1 BOTTLE, PLASTIC (43063-861-98)
source: ndc

Packages (6)

43063-861-14 14 TABLET in 1 BOTTLE, PLASTIC (43063-861-14) 43063-861-30 30 TABLET in 1 BOTTLE, PLASTIC (43063-861-30) 43063-861-60 60 TABLET in 1 BOTTLE, PLASTIC (43063-861-60) 43063-861-90 90 TABLET in 1 BOTTLE, PLASTIC (43063-861-90) 43063-861-93 180 TABLET in 1 BOTTLE, PLASTIC (43063-861-93) 43063-861-98 120 TABLET in 1 BOTTLE, PLASTIC (43063-861-98)

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": "3a212166-4cbf-fa96-e063-6394a90a5cd2", "openfda": {"nui": ["N0000175608", "M0020795"], "upc": ["0343063861301"], "unii": ["X7WDT95N5C"], "rxcui": ["310488"], "spl_set_id": ["1b2e5656-9da9-4fab-bf01-ed75896b836a"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (43063-861-14)", "package_ndc": "43063-861-14", "marketing_start_date": "20180612"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-861-30)", "package_ndc": "43063-861-30", "marketing_start_date": "20180612"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (43063-861-60)", "package_ndc": "43063-861-60", "marketing_start_date": "20180612"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43063-861-90)", "package_ndc": "43063-861-90", "marketing_start_date": "20180612"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE, PLASTIC (43063-861-93)", "package_ndc": "43063-861-93", "marketing_start_date": "20180612"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE, PLASTIC (43063-861-98)", "package_ndc": "43063-861-98", "marketing_start_date": "20180612"}], "brand_name": "Glipizide", "product_id": "43063-861_3a212166-4cbf-fa96-e063-6394a90a5cd2", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "43063-861", "generic_name": "Glipizide", "labeler_name": "PD-Rx Pharmaceuticals, 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": "20020925", "listing_expiration_date": "20261231"}