Pomalidomide
- Product NDC
- 0480-4035
- 11-digit product format
- 004804035
- Labeler code
- 0480
- Product ID
- 0480-4035_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
- 4 mg/1
- Pharmacologic classes
- Thalidomide Analog [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Pomalidomide
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| POMALIDOMIDE | 4 mg/1 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0480-4035-21 | Pomalidomide | 21 in 1 BOTTLE | CAPSULE | 21 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0480-4035-21 | 00480403521 | 21 CAPSULE in 1 BOTTLE (0480-4035-21) | 21 capsule | 2026-03-02 | No | No | Current |