plerixafor
- Product NDC
- 70121-1694
- 11-digit product format
- 701211694
- Labeler code
- 70121
- Product ID
- 70121-1694_f578a658-ea16-45b4-9e4f-4eddad5e873b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- plerixafor
- Dosage form
- INJECTION, SOLUTION
- Route
- SUBCUTANEOUS
- Labeler
- Amneal Pharmaceuticals LLC
- Application
- ANDA215334
- Marketing category
- ANDA
- Marketing start
- 2023-07-25
- Substance
- PLERIXAFOR
- Active strength
- 24 mg/1.2mL
- Pharmacologic classes
- Hematopoietic Stem Cell Mobilizer [EPC], Increased Hematopoietic Stem Cell Mobilization [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- plerixafor
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PLERIXAFOR | 24 mg/1.2mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | S915P5499N |
| Rxcui | 828700 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70121-1694-2 | plerixafor | 1.2 mL in 1 VIAL, SINGLE-DOSE | INJECTION, SOLUTION | 1.2 | | 4 |
| 70121-1694-2 | plerixafor | 1 in 1 CARTON | INJECTION, SOLUTION | 1 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70121-1694 | PLERIXAFOR INJECTION, SOLUTION [AMNEAL PHARMACEUTICALS LLC] | 4 | Current NDC, 2 package rows | 20240302_d3f32914-4be5-4455-a3db-36c652051cf5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 70121-1694-2 | 70121169402 | 1 VIAL, SINGLE-DOSE in 1 CARTON (70121-1694-2) / 1.2 mL in 1 VIAL, SINGLE-DOSE | 2023-07-25 | No | No | Historical |