LEVOLEUCOVORIN
- Product NDC
- 16714-890
- 11-digit product format
- 167140890
- Labeler code
- 16714
- Product ID
- 16714-890_a133917e-1ae8-1bbd-152b-58a5a07769b7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LEVOLEUCOVORIN
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- NorthStar RxLLC
- Application
- ANDA210892
- Marketing category
- ANDA
- Marketing start
- 2018-09-26
- Marketing end
- 0000-00-00
- Substance
- LEVOLEUCOVORIN CALCIUM
- Active strength
- 175 mg/17.5mL
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16714-890-01 | 16714089001 | 1 VIAL, SINGLE-DOSE in 1 CARTON (16714-890-01) > 17.5 mL in 1 VIAL, SINGLE-DOSE | 2018-09-26 | 0000-00-00 | No | No | Current |