NDC 70518-2129-00 - Pioglitazone

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
70518-2129
Requested NDC
70518-2129-00
Package NDCs from labels
70518-2129-0, 70518-2129-00
Manufacturer
REMEDYREPACK INC.
Effective date
2026-01-30
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Pioglitazone - REMEDYREPACK INC.REMEDYREPACK INC.2026-01-30HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70518-2129-0Pioglitazone90 in 1 BOTTLE, PLASTICTABLET9012

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70518-2129PIOGLITAZONE TABLET [REMEDYREPACK INC.]10Current NDC, Legacy NDC, 1 package rows20250308_55f9b2d8-3e78-4e2f-bcf1-d00595078fa1.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 3 of 3 · 53 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
PioglitazonePIOGLITAZONENuCare Pharmaceuticals,Inc.a1112e4b-e9d5-13c3-e053-2995a90a6d0a2024-06-20Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA200268
rxcui: 312440
unii: JQT35NPK6C
PioglitazonePIOGLITAZONENuCare Pharmaceuticals,Inc.a0846e3e-68b2-fd55-e053-2995a90a673e2024-06-20Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA200268
rxcui: 317573
unii: JQT35NPK6C
PioglitazonePIOGLITAZONENuCare Pharmaceuticals,Inc.8d5ac747-991f-30e4-e053-2a95a90a47802024-06-18Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA200268
rxcui: 312440
unii: JQT35NPK6C
PioglitazonePIOGLITAZONEProficient Rx LPf725cdaf-fc7a-40d6-ba64-1dccd1b25d7a2024-06-01Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA200268
rxcui: 312440
unii: JQT35NPK6C
PioglitazonePIOGLITAZONEA-S Medication Solutions9fe57786-5c7d-4b11-8fb4-de341e2e51282023-12-05Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 312440
unii: JQT35NPK6C
PioglitazonePIOGLITAZONEA-S Medication Solutions4b5506c4-8cc2-44fb-ba2b-0e29fb73943d2023-12-05Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 312440
unii: JQT35NPK6C
PioglitazonePIOGLITAZONEA-S Medication Solutions475c4f39-dd2a-48f9-a07c-9344bbda58a92023-04-04Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 312441
unii: JQT35NPK6C
PioglitazonePIOGLITAZONEA-S Medication Solutions5f844e44-0f0d-4b28-9d34-b97780e1c6ec2023-02-06Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA200268
rxcui: 317573
unii: JQT35NPK6C
PioglitazonePIOGLITAZONEMacleods Pharmaceuticals Limited482cef76-0623-4b4f-a0ea-f008c97b22812022-12-26Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 312441
rxcui: 312440
rxcui: 317573
unii: JQT35NPK6C
PioglitazonePIOGLITAZONENorthStar RxLLC692e662a-3b31-42c3-a075-42abe44c74db2022-09-08Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 312441
rxcui: 312440
rxcui: 317573
unii: JQT35NPK6C
PioglitazonePIOGLITAZONETeva Pharmaceuticals USA, Inc.c5c81c67-90cf-4e64-acb5-58b0358fa7422021-07-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 312441
rxcui: 312440
rxcui: 317573
unii: JQT35NPK6C
PioglitazonePIOGLITAZONEAphena Pharma Solutions - Tennessee, LLCf434ba0d-13f3-42ae-a2d5-cddb93fde1e82020-12-16Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA200268
rxcui: 317573
unii: JQT35NPK6C
PIOGLITAZONEPIOGLITAZONESolco Healthcare LLC1b77dbeb-61d1-4df3-872b-2f4f75a110db2020-01-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 312441
rxcui: 312440
rxcui: 317573

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.