acarbose

Generic: acarbose

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

Drug Facts

Product Profile

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

acarbose 50 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-132
Product ID 72789-132_2c2501a6-a6d6-1d6c-e063-6294a90ad428
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078470
Listing Expiration 2026-12-31
Marketing Start 2008-05-07

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 72789132
Hyphenated Format 72789-132

Supplemental Identifiers

RxCUI
199149 199150 200132
UPC
0372789133904 0372789131306 0372789132600
UNII
T58MSI464G
NUI
N0000000166 N0000175559

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 ANDA078470 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (72789-132-30)
  • 60 TABLET in 1 BOTTLE, PLASTIC (72789-132-60)
  • 90 TABLET in 1 BOTTLE, PLASTIC (72789-132-90)
source: ndc

Packages (3)

72789-132-30 30 TABLET in 1 BOTTLE, PLASTIC (72789-132-30) 72789-132-60 60 TABLET in 1 BOTTLE, PLASTIC (72789-132-60) 72789-132-90 90 TABLET in 1 BOTTLE, PLASTIC (72789-132-90)

Ingredients (1)

acarbose (50 mg/1)

Linked Drug Pages (1)

Acarbose ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c2501a6-a6d6-1d6c-e063-6294a90ad428", "openfda": {"nui": ["N0000000166", "N0000175559"], "upc": ["0372789133904", "0372789131306", "0372789132600"], "unii": ["T58MSI464G"], "rxcui": ["199149", "199150", "200132"], "spl_set_id": ["722ce9eb-8f7b-4651-a287-d53dd7ab3707"], "pharm_class_epc": ["alpha-Glucosidase Inhibitor [EPC]"], "pharm_class_moa": ["alpha Glucosidase Inhibitors [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-132-30)", "package_ndc": "72789-132-30", "marketing_start_date": "20230707"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (72789-132-60)", "package_ndc": "72789-132-60", "marketing_start_date": "20201021"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-132-90)", "package_ndc": "72789-132-90", "marketing_start_date": "20220916"}], "brand_name": "Acarbose", "product_id": "72789-132_2c2501a6-a6d6-1d6c-e063-6294a90ad428", "dosage_form": "TABLET", "pharm_class": ["alpha Glucosidase Inhibitors [MoA]", "alpha-Glucosidase Inhibitor [EPC]"], "product_ndc": "72789-132", "generic_name": "Acarbose", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acarbose", "active_ingredients": [{"name": "ACARBOSE", "strength": "50 mg/1"}], "application_number": "ANDA078470", "marketing_category": "ANDA", "marketing_start_date": "20080507", "listing_expiration_date": "20261231"}