Oxaliplatin
- Product NDC
- 72266-162
- 11-digit product format
- 722660162
- Labeler code
- 72266
- Product ID
- 72266-162_2b48f7c2-8c48-6b82-e063-6394a90a3baf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxaliplatin
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- FOSUN PHARMA USA INC.
- Application
- ANDA207325
- Marketing category
- ANDA
- Marketing start
- 2020-03-30
- 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 |
|---|
| 72266-162-01 | Oxaliplatin | 20 mL in 1 VIAL, SINGLE-USE | INJECTION, SOLUTION | 20 | | 6 |
| 72266-162-01 | Oxaliplatin | 1 in 1 CARTON | INJECTION, SOLUTION | 1 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72266-162 | OXALIPLATIN INJECTION, SOLUTION [FOSUN PHARMA USA INC.] | 6 | Current NDC, Legacy NDC, 2 package rows | 20250205_fad0f147-6595-4412-87a7-2afca0192a96.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 |
|---|
| 72266-162-01 | 72266016201 | 1 VIAL, SINGLE-USE in 1 CARTON (72266-162-01) / 20 mL in 1 VIAL, SINGLE-USE | 2020-03-30 | 0000-00-00 | No | No | Current |