acarbose

Generic: acarbose

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acarbose
Generic Name acarbose
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acarbose 25 mg/1

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-147
Product ID 23155-147_54493f37-e851-40e4-83e0-6f16eddc8b04
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202271
Listing Expiration 2026-12-31
Marketing Start 2021-04-16

Pharmacologic Class

Established (EPC)
alpha-glucosidase inhibitor [epc]
Mechanism of Action
alpha glucosidase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 23155147
Hyphenated Format 23155-147

Supplemental Identifiers

RxCUI
199149 199150 200132
UNII
T58MSI464G
NUI
N0000000166 N0000175559

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 acarbose (source: ndc)
Generic Name acarbose (source: ndc)
Application Number ANDA202271 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (23155-147-01)
  • 500 TABLET in 1 BOTTLE (23155-147-05)
  • 1000 TABLET in 1 BOTTLE (23155-147-10)
source: ndc

Packages (3)

Ingredients (1)

acarbose (25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "54493f37-e851-40e4-83e0-6f16eddc8b04", "openfda": {"nui": ["N0000000166", "N0000175559"], "unii": ["T58MSI464G"], "rxcui": ["199149", "199150", "200132"], "spl_set_id": ["29939129-7d09-4c22-bf3e-491a8a97f4c4"], "pharm_class_epc": ["alpha-Glucosidase Inhibitor [EPC]"], "pharm_class_moa": ["alpha Glucosidase Inhibitors [MoA]"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (23155-147-01)", "package_ndc": "23155-147-01", "marketing_start_date": "20210416"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (23155-147-05)", "package_ndc": "23155-147-05", "marketing_start_date": "20210416"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (23155-147-10)", "package_ndc": "23155-147-10", "marketing_start_date": "20210416"}], "brand_name": "Acarbose", "product_id": "23155-147_54493f37-e851-40e4-83e0-6f16eddc8b04", "dosage_form": "TABLET", "pharm_class": ["alpha Glucosidase Inhibitors [MoA]", "alpha-Glucosidase Inhibitor [EPC]"], "product_ndc": "23155-147", "generic_name": "Acarbose", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acarbose", "active_ingredients": [{"name": "ACARBOSE", "strength": "25 mg/1"}], "application_number": "ANDA202271", "marketing_category": "ANDA", "marketing_start_date": "20210416", "listing_expiration_date": "20261231"}