glimepiride 3 mg

Generic: glimepiride

Labeler: lifsa drugs llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name glimepiride 3 mg
Generic Name glimepiride
Labeler lifsa drugs llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

glimepiride 3 mg/1

Manufacturer
Lifsa Drugs LLC

Identifiers & Regulatory

Product NDC 72336-641
Product ID 72336-641_8f56950f-d08d-44d4-9c7c-9830e9bfadb8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091220
Listing Expiration 2026-12-31
Marketing Start 2024-08-20

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72336641
Hyphenated Format 72336-641

Supplemental Identifiers

RxCUI
153842
UPC
0372336641012
UNII
6KY687524K
NUI
N0000175608 M0020795

Packaging Origin

Original Packager
true

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 glimepiride 3 mg (source: ndc)
Generic Name glimepiride (source: ndc)
Application Number ANDA091220 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 3 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72336-641-01)
source: ndc

Packages (1)

Ingredients (1)

glimepiride (3 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8f56950f-d08d-44d4-9c7c-9830e9bfadb8", "openfda": {"nui": ["N0000175608", "M0020795"], "upc": ["0372336641012"], "unii": ["6KY687524K"], "rxcui": ["153842"], "spl_set_id": ["51157849-7990-4a8b-ae50-eda1baf93cfa"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Lifsa Drugs LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72336-641-01)", "package_ndc": "72336-641-01", "marketing_start_date": "20240820"}], "brand_name": "Glimepiride 3 mg", "product_id": "72336-641_8f56950f-d08d-44d4-9c7c-9830e9bfadb8", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "72336-641", "generic_name": "Glimepiride", "labeler_name": "Lifsa Drugs LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glimepiride 3 mg", "active_ingredients": [{"name": "GLIMEPIRIDE", "strength": "3 mg/1"}], "application_number": "ANDA091220", "marketing_category": "ANDA", "marketing_start_date": "20240820", "listing_expiration_date": "20261231"}