Pioglitazone hydrochloride and glimepiride
- Product NDC
- 0781-5634
- 11-digit product format
- 007815634
- Labeler code
- 0781
- Product ID
- 0781-5634_724cb72e-023e-409c-8979-3a380a2fdc0a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pioglitazone hydrochloride and glimepiride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- ANDA201049
- Marketing category
- ANDA
- Marketing start
- 2013-01-08
- Marketing end
- 0000-00-00
- Substance
- PIOGLITAZONE HYDROCHLORIDE; GLIMEPIRIDE
- Active strength
- 30 mg/1; 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],Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 0781-5634-10 | 00781563410 | 1000 TABLET in 1 BOTTLE (0781-5634-10) | 1000 tablet | 2013-01-08 | 0000-00-00 | No | No | Current |
| 0781-5634-31 | 00781563431 | 30 TABLET in 1 BOTTLE (0781-5634-31) | 30 tablet | 2013-01-08 | 0000-00-00 | No | No | Current |