acarbose

Generic: acarbose

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acarbose
Generic Name acarbose
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acarbose 50 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-9725
Product ID 71335-9725_5b695702-3a0b-4370-a452-7894329970ba
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 713359725
Hyphenated Format 71335-9725

Supplemental Identifiers

RxCUI
199149
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 ANDA202271 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-9725-1)
  • 90 TABLET in 1 BOTTLE (71335-9725-2)
  • 100 TABLET in 1 BOTTLE (71335-9725-3)
source: ndc

Packages (3)

71335-9725-1 30 TABLET in 1 BOTTLE (71335-9725-1) 71335-9725-2 90 TABLET in 1 BOTTLE (71335-9725-2) 71335-9725-3 100 TABLET in 1 BOTTLE (71335-9725-3)

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": "5b695702-3a0b-4370-a452-7894329970ba", "openfda": {"nui": ["N0000000166", "N0000175559"], "unii": ["T58MSI464G"], "rxcui": ["199149"], "spl_set_id": ["067c0adc-7322-489d-9baa-1d061b37be36"], "pharm_class_epc": ["alpha-Glucosidase Inhibitor [EPC]"], "pharm_class_moa": ["alpha Glucosidase Inhibitors [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-9725-1)", "package_ndc": "71335-9725-1", "marketing_start_date": "20230911"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-9725-2)", "package_ndc": "71335-9725-2", "marketing_start_date": "20240812"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-9725-3)", "package_ndc": "71335-9725-3", "marketing_start_date": "20240812"}], "brand_name": "Acarbose", "product_id": "71335-9725_5b695702-3a0b-4370-a452-7894329970ba", "dosage_form": "TABLET", "pharm_class": ["alpha Glucosidase Inhibitors [MoA]", "alpha-Glucosidase Inhibitor [EPC]"], "product_ndc": "71335-9725", "generic_name": "Acarbose", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acarbose", "active_ingredients": [{"name": "ACARBOSE", "strength": "50 mg/1"}], "application_number": "ANDA202271", "marketing_category": "ANDA", "marketing_start_date": "20210416", "listing_expiration_date": "20261231"}