vigabatrin
- Product NDC
- 70771-1742
- 11-digit product format
- 707711742
- Labeler code
- 70771
- Product ID
- 70771-1742_2fd46d14-d59a-4335-9f92-9e029defc7b2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- vigabatrin
- Dosage form
- POWDER, FOR SOLUTION
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA214671
- Marketing category
- ANDA
- Marketing start
- 2025-03-24
- Substance
- VIGABATRIN
- Active strength
- 500 mg/10mL
- Pharmacologic classes
- Anti-epileptic Agent [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- vigabatrin
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| VIGABATRIN | 500 mg/10mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | GR120KRT6K |
| Rxcui | 250820 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70771-1742-1 | vigabatrin | 10 mL in 1 PACKET | POWDER, FOR SOLUTION | 10 | | 2 |
| 70771-1742-8 | vigabatrin | 50 in 1 CARTON | POWDER, FOR SOLUTION | 50 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70771-1742 | VIGABATRIN POWDER, FOR SOLUTION [ZYDUS LIFESCIENCES LIMITED] | 1 | Current NDC, 2 package rows | 20250325_cd5ebc7a-8d5b-46b4-ad9b-e4a25fa3e26c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70771-1742-1 | 70771174201 | 10 mL in 1 PACKET | 10 ml | | | | Historical |
| 70771-1742-8 | 70771174208 | 50 PACKET in 1 CARTON (70771-1742-8) / 10 mL in 1 PACKET (70771-1742-1) | 50 packet | 2025-03-24 | No | No | Historical |