Pomalidomide
- Product NDC
- 0480-4018
- 11-digit product format
- 004804018
- Labeler code
- 0480
- Product ID
- 0480-4018_b6e6a69c-e11e-4eb7-9340-4eb92255f400
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pomalidomide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals, Inc.
- Application
- ANDA209956
- Marketing category
- ANDA
- Marketing start
- 2026-03-02
- Substance
- POMALIDOMIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Thalidomide Analog [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| D2UX06XLB5 | POMALIDOMIDE | 19171-19-8 | POMALIDOMIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0480-4018-21 | 00480401821 | 21 CAPSULE in 1 BOTTLE (0480-4018-21) | 21 capsule | 2026-03-02 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Pomalidomide | Teva Pharmaceuticals, Inc. | 2026-03-02 | HUMAN PRESCRIPTION DRUG LABEL | 1 |