levetiracetam
- Product NDC
- 68180-099
- 11-digit product format
- 681800099
- Labeler code
- 68180
- Product ID
- 68180-099_b563e4c3-b25b-4b71-8bba-99fee0511fee
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- levetiracetam
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Lupin Pharmaceuticals, Inc.
- Application
- ANDA090893
- Marketing category
- ANDA
- Marketing start
- 2014-11-01
- Marketing end
- 0000-00-00
- Substance
- LEVETIRACETAM
- Active strength
- 100 mg/mL
- Pharmacologic classes
- Decreased Central Nervous System Disorganized Electrical Activity [PE]
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68180-099-01 | 68180009901 | 473 mL in 1 BOTTLE (68180-099-01) | 473 ml | 2014-11-01 | 0000-00-00 | No | No | Current |