LEVETIRACETAM
- Product NDC
- 27241-008
- 11-digit product format
- 272410008
- Labeler code
- 27241
- Product ID
- 27241-008_0335364f-0704-41c8-8a1b-3120a7ad414b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LEVETIRACETAM
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Ajanta Pharma Limited
- Application
- ANDA201293
- Marketing category
- ANDA
- Marketing start
- 2011-06-14
- Marketing end
- 0000-00-00
- Substance
- LEVETIRACETAM
- Active strength
- 500 mg/1
- Pharmacologic classes
- Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 27241-008-12 | LEVETIRACETAM | 120 in 1 BOTTLE | TABLET, FILM COATED | 120 | | 22 |
| 27241-008-50 | LEVETIRACETAM | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | | 22 |
| 27241-008-90 | LEVETIRACETAM | 1000 in 1 BOTTLE | TABLET, FILM COATED | 1000 | | 22 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 27241-008 | LEVETIRACETAM TABLET, FILM COATED [AJANTA PHARMA LIMITED] | 22 | Legacy NDC, 3 package rows | 20171204_43fe36cf-5146-46b8-8a24-b38591aee6b4.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 27241-008-12 | 27241000812 | 120 in 1 BOTTLE | Historical |
| 27241-008-50 | 27241000850 | 500 in 1 BOTTLE | Historical |
| 27241-008-90 | 27241000890 | 1000 in 1 BOTTLE | Historical |