pioglitazone and metformin hydrochloride

Generic: pioglitazone and metformin hydrochloride

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

Drug Facts

Product Profile

Brand Name pioglitazone and metformin hydrochloride
Generic Name pioglitazone and metformin hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

metformin hydrochloride 500 mg/1, pioglitazone hydrochloride 15 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-3019
Product ID 71335-3019_7c59377b-a0cb-48b3-af4f-95f64d0f4ad1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204802
Listing Expiration 2026-12-31
Marketing Start 2015-11-06

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs] peroxisome proliferator receptor alpha agonist [epc] peroxisome proliferator receptor gamma agonist [epc] peroxisome proliferator-activated receptor alpha agonists [moa] peroxisome proliferator-activated receptor gamma agonists [moa] thiazolidinedione [epc] thiazolidinediones [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713353019
Hyphenated Format 71335-3019

Supplemental Identifiers

RxCUI
861783
UNII
786Z46389E JQT35NPK6C

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 pioglitazone and metformin hydrochloride (source: ndc)
Generic Name pioglitazone and metformin hydrochloride (source: ndc)
Application Number ANDA204802 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
  • 15 mg/1
source: ndc
Packaging
  • 180 TABLET in 1 BOTTLE (71335-3019-1)
source: ndc

Packages (1)

71335-3019-1 180 TABLET in 1 BOTTLE (71335-3019-1)

Ingredients (2)

metformin hydrochloride (500 mg/1) pioglitazone hydrochloride (15 mg/1)

Linked Drug Pages (1)

Pioglitazone and metformin hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7c59377b-a0cb-48b3-af4f-95f64d0f4ad1", "openfda": {"unii": ["786Z46389E", "JQT35NPK6C"], "rxcui": ["861783"], "spl_set_id": ["8080eedb-e955-4059-98b2-9685b608eb3e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET in 1 BOTTLE (71335-3019-1)", "package_ndc": "71335-3019-1", "marketing_start_date": "20251203"}], "brand_name": "Pioglitazone and metformin hydrochloride", "product_id": "71335-3019_7c59377b-a0cb-48b3-af4f-95f64d0f4ad1", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]", "Peroxisome Proliferator Receptor alpha Agonist [EPC]", "Peroxisome Proliferator Receptor gamma Agonist [EPC]", "Peroxisome Proliferator-activated Receptor alpha Agonists [MoA]", "Peroxisome Proliferator-activated Receptor gamma Agonists [MoA]", "Thiazolidinedione [EPC]", "Thiazolidinediones [CS]"], "product_ndc": "71335-3019", "generic_name": "Pioglitazone and metformin hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pioglitazone and metformin hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}, {"name": "PIOGLITAZONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA204802", "marketing_category": "ANDA", "marketing_start_date": "20151106", "listing_expiration_date": "20261231"}