Pomalidomide
- Product NDC
- 60505-4499
- 11-digit product format
- 605054499
- Labeler code
- 60505
- Product ID
- 60505-4499_79028ff4-3130-88ed-e3fc-18a7d9a779b8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pomalidomide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Apotex Corp.
- Application
- ANDA210164
- Marketing category
- ANDA
- Marketing start
- 2026-03-11
- Substance
- POMALIDOMIDE
- Active strength
- 3 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 | 3 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | D2UX06XLB5 |
| Rxcui | 1369718, 1369726, 1369730, 1369734 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60505-4499-1 | Pomalidomide | 100 in 1 BOTTLE | CAPSULE | 100 | | 2 |
| 60505-4499-2 | Pomalidomide | 21 in 1 BOTTLE | CAPSULE | 21 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 60505-4499-1 | 60505449901 | 100 in 1 BOTTLE | | | | | Historical |
| 60505-4499-2 | 60505449902 | 21 CAPSULE in 1 BOTTLE (60505-4499-2) | 21 capsule | 2026-03-11 | No | No | Historical |