Oxaliplatin
- Product NDC
- 43066-014
- 11-digit product format
- 430660014
- Labeler code
- 43066
- Product ID
- 43066-014_e6815a98-0efc-4d69-8612-9e7ab7e78c0a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxaliplatin
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Baxter Healthcare Corporation
- Application
- ANDA078817
- Marketing category
- ANDA
- Marketing start
- 2018-02-19
- Substance
- OXALIPLATIN
- Active strength
- 5 mg/mL
- Pharmacologic classes
- Platinum-based Drug [EPC], Platinum-containing Compounds [EXT]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Oxaliplatin
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OXALIPLATIN | 5 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 04ZR38536J |
| Rxcui | 1736776, 1736781 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 43066-014-01 | Oxaliplatin | 10 mL in 1 VIAL, SINGLE-USE | INJECTION, SOLUTION | 10 | | 7 |
| 43066-014-01 | Oxaliplatin | 1 in 1 CARTON | INJECTION, SOLUTION | 1 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43066-014 | OXALIPLATIN INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION] | 7 | Current NDC, Legacy NDC, 2 package rows | 20250130_21a2bb1d-d91d-4f99-97dd-cc67fe99a090.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43066-014-01 | 43066001401 | 1 VIAL, SINGLE-USE in 1 CARTON (43066-014-01) / 10 mL in 1 VIAL, SINGLE-USE | 2018-02-19 | 0000-00-00 | No | No | Current |