Pioglitazone Hydrochloride
- Product NDC
- 70518-1638
- 11-digit product format
- 705181638
- Labeler code
- 70518
- Product ID
- 70518-1638_e87c1cfc-bca7-f7a4-e053-2995a90a8f03
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pioglitazone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA200044
- Marketing category
- ANDA
- Marketing start
- 2018-11-06
- Marketing end
- 0000-00-00
- Substance
- PIOGLITAZONE HYDROCHLORIDE
- Active strength
- 30 mg/1
- Pharmacologic classes
- PPAR alpha [CS], PPAR gamma [CS], Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator Receptor gamma Agonist [EPC], Peroxisome Proliferator-activated Receptor Activity [MoA], Thiazolidinedione [EPC], Thiazolidinediones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-1638 | PIOGLITAZONE HYDROCHLORIDE TABLET [REMEDYREPACK INC.] | 9 | Legacy NDC | 20240615_55ae23ff-60f5-4de6-bd1b-472243b8636b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1638-0 | 70518163800 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-1638-0) | 90 tablet | 2018-11-06 | 0000-00-00 | No | No | Current |