Pioglitazone
- Product NDC
- 70518-2431
- 11-digit product format
- 705182431
- Labeler code
- 70518
- Product ID
- 70518-2431_dbd872ce-ef3b-541a-e053-2a95a90a091b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pioglitazone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA200268
- Marketing category
- ANDA
- Marketing start
- 2019-11-18
- Marketing end
- 0000-00-00
- Substance
- PIOGLITAZONE HYDROCHLORIDE
- Active strength
- 45 mg/1
- Pharmacologic classes
- PPAR alpha [CS], PPAR gamma [CS], Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator Receptor gamma Agonist [EPC], Peroxisome Proliferator-activated Receptor Activity [MoA], Thiazolidinedione [EPC], Thiazolidinediones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-2431 | PIOGLITAZONE TABLET [REMEDYREPACK INC.] | 9 | Legacy NDC | 20250316_db4564ed-1595-403a-a20d-8dad515c9e56.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2431-0 | 70518243100 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-2431-0) | 90 tablet | 2019-11-18 | 0000-00-00 | No | No | Current |
| 70518-2431-1 | 70518243101 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-2431-1) | 90 tablet | 2021-09-23 | 0000-00-00 | No | No | Current |