Pioglitazone Hydrochloride
- Product NDC
- 68788-6846
- 11-digit product format
- 687886846
- Labeler code
- 68788
- Product ID
- 68788-6846_021be560-f1b6-4364-8e62-b8ffe6bd1551
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- pioglitazone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA200044
- Marketing category
- ANDA
- Marketing start
- 2016-12-07
- Marketing end
- 0000-00-00
- Substance
- PIOGLITAZONE HYDROCHLORIDE
- Active strength
- 30 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 |
|---|
| 68788-6846-1 | 68788684601 | 100 TABLET in 1 BOTTLE (68788-6846-1) | 100 tablet | 2016-12-07 | 0000-00-00 | No | No | Current |
| 68788-6846-3 | 68788684603 | 30 TABLET in 1 BOTTLE (68788-6846-3) | 30 tablet | 2016-12-07 | 0000-00-00 | No | No | Current |
| 68788-6846-6 | 68788684606 | 60 TABLET in 1 BOTTLE (68788-6846-6) | 60 tablet | 2016-12-07 | 0000-00-00 | No | No | Current |
| 68788-6846-9 | 68788684609 | 90 TABLET in 1 BOTTLE (68788-6846-9) | 90 tablet | 2016-12-07 | 0000-00-00 | No | No | Current |