Pioglitazone
- Product NDC
- 82804-111
- 11-digit product format
- 828040111
- Labeler code
- 82804
- Product ID
- 82804-111_f725cdaf-fc7a-40d6-ba64-1dccd1b25d7a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pioglitazone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA200268
- Marketing category
- ANDA
- Marketing start
- 2013-02-13
- Substance
- PIOGLITAZONE HYDROCHLORIDE
- Active strength
- 30 mg/1
- Pharmacologic classes
- Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator Receptor gamma Agonist [EPC], Peroxisome Proliferator-activated Receptor alpha Agonists [MoA], Peroxisome Proliferator-activated Receptor gamma Agonists [MoA], Thiazolidinedione [EPC], Thiazolidinediones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| JQT35NPK6C | PIOGLITAZONE HYDROCHLORIDE | 112529-15-4 | PIOGLITAZONE HYDROCHLORIDE |
| X4OV71U42S | PIOGLITAZONE | 111025-46-8 | Pioglitazone |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82804-111-30 | 82804011130 | 30 TABLET in 1 BOTTLE (82804-111-30) | 30 tablet | 2024-06-20 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Pioglitazone | Proficient Rx LP | 2024-06-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |