Pioglitazone
- Product NDC
- 71335-1659
- 11-digit product format
- 713351659
- Labeler code
- 71335
- Product ID
- 71335-1659_c2ec028e-5710-4a4d-98b1-c8eef3b90c13
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- pioglitazone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078670
- Marketing category
- ANDA
- Marketing start
- 2013-03-01
- Marketing end
- 0000-00-00
- Substance
- PIOGLITAZONE HYDROCHLORIDE
- Active strength
- 15 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71335-1659 | PIOGLITAZONE TABLET [BRYANT RANCH PREPACK] | 1 | Legacy NDC | 20200919_fc5ea675-0eb5-42dd-a33f-46d5fda1517c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1659-1 | 71335165901 | 30 TABLET in 1 BOTTLE (71335-1659-1) | 30 tablet | 2020-07-08 | 0000-00-00 | No | No | Current |
| 71335-1659-2 | 71335165902 | 90 TABLET in 1 BOTTLE (71335-1659-2) | 90 tablet | 2020-07-08 | 0000-00-00 | No | No | Current |
| 71335-1659-3 | 71335165903 | 60 TABLET in 1 BOTTLE (71335-1659-3) | 60 tablet | 2020-07-08 | 0000-00-00 | No | No | Current |
| 71335-1659-4 | 71335165904 | 120 TABLET in 1 BOTTLE (71335-1659-4) | 120 tablet | 2020-07-08 | 0000-00-00 | No | No | Current |