Pioglitazone Hydrochloride
- Product NDC
- 68788-6888
- 11-digit product format
- 687886888
- Labeler code
- 68788
- Product ID
- 68788-6888_e220d648-c9da-4105-8219-91e488f4d3a8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- pioglitazone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA200044
- Marketing category
- ANDA
- Marketing start
- 2017-02-01
- 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
- 2022-12-31
- 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 |
|---|
| 68788-6888-1 | 68788688801 | 100 TABLET in 1 BOTTLE (68788-6888-1) | 100 tablet | 2017-02-01 | 0000-00-00 | No | No | Current |
| 68788-6888-3 | 68788688803 | 30 TABLET in 1 BOTTLE (68788-6888-3) | 30 tablet | 2017-02-01 | 0000-00-00 | No | No | Current |
| 68788-6888-6 | 68788688806 | 60 TABLET in 1 BOTTLE (68788-6888-6) | 60 tablet | 2017-02-01 | 0000-00-00 | No | No | Current |
| 68788-6888-9 | 68788688809 | 90 TABLET in 1 BOTTLE (68788-6888-9) | 90 tablet | 2017-02-01 | 0000-00-00 | No | No | Current |