Pioglitazone
- Product NDC
- 71335-0088
- 11-digit product format
- 713350088
- Labeler code
- 71335
- Product ID
- 71335-0088_785da36d-66bc-419b-957c-69427d0b29db
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pioglitazone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202467
- Marketing category
- ANDA
- Marketing start
- 2013-02-14
- Marketing end
- 0000-00-00
- Substance
- PIOGLITAZONE HYDROCHLORIDE
- Active strength
- 45 mg/1
- Pharmacologic classes
- Peroxisome Proliferator-activated Receptor Activity [MoA],PPAR alpha [CS],PPAR gamma [CS],Thiazolidinedione [EPC],Thiazolidinediones [CS],Peroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator Receptor gamma Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0088-1 | 71335008801 | 30 TABLET in 1 BOTTLE (71335-0088-1) | 30 tablet | 2017-08-17 | 0000-00-00 | No | No | Current |
| 71335-0088-2 | 71335008802 | 90 TABLET in 1 BOTTLE (71335-0088-2) | 90 tablet | 2017-08-17 | 0000-00-00 | No | No | Current |