Levoleucovorin
- Product NDC
- 70121-1099
- 11-digit product format
- 701211099
- Labeler code
- 70121
- Product ID
- 70121-1099_e5de95c2-e701-4b6d-a8e8-5c04bb882680
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levoleucovorin
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Amneal Pharmaceuticals LLC
- Application
- ANDA207547
- Marketing category
- ANDA
- Marketing start
- 2017-02-13
- Marketing end
- 0000-00-00
- Substance
- LEVOLEUCOVORIN CALCIUM
- Active strength
- 50 mg/1
- Pharmacologic classes
- Folate Analog [EPC], Folic Acid [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70121-1099 | LEVOLEUCOVORIN INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [AMNEAL PHARMACEUTICALS LLC] | 15 | Legacy NDC | 20240810_23efb660-8c30-4d9c-99e7-31d982884e76.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70121-1099-1 | 70121109901 | 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (70121-1099-1) | 2017-02-13 | 0000-00-00 | No | No | Current |