Levetiracetam
- Product NDC
- 43598-755
- 11-digit product format
- 435980755
- Labeler code
- 43598
- Product ID
- 43598-755_b6d4150a-3849-e804-02cb-468a6593dd71
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levetiracetam Injection
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Dr.Reddy's Laboratories Inc
- Application
- ANDA206880
- Marketing category
- ANDA
- Marketing start
- 2018-06-08
- Substance
- LEVETIRACETAM
- Active strength
- 5 mg/mL
- Pharmacologic classes
- Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 44YRR34555 | LEVETIRACETAM | 102767-28-2 | LEVETIRACETAM |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 43598-755-10 | 43598075510 | 10 BAG in 1 CARTON (43598-755-10) / 100 mL in 1 BAG (43598-755-52) | 10 bag | 2018-06-08 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Levetiracetam Injection | Dr.Reddy's Laboratories Inc | GLAND PHARMA LIMITED | 2021-12-31 | HUMAN PRESCRIPTION DRUG LABEL | 3 |