Levoleucovorin
- Product NDC
- 0781-3201
- 11-digit product format
- 007813201
- Labeler code
- 0781
- Product ID
- 0781-3201_ebd9643f-c9f0-4815-b7c0-3ff64cce651b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levoleucovorin
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Sandoz Inc
- Application
- ANDA203563
- Marketing category
- ANDA
- Marketing start
- 2015-04-23
- Marketing end
- 0000-00-00
- Substance
- LEVOLEUCOVORIN CALCIUM PENTAHYDRATE
- Active strength
- 175 mg/17.5mL
- Pharmacologic classes
- Folate Analog [EPC],Folic Acid [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0781-3201-94 | 00781320194 | 1 VIAL, SINGLE-USE in 1 CARTON (0781-3201-94) > 17.5 mL in 1 VIAL, SINGLE-USE | 2015-04-23 | 0000-00-00 | No | No | Current |