NDC 51672-4172 – Felbamate
Felbamate 600 mg/5mL · Suspension · Oral
Product NDC51672-4172
Product details
- Brand name
- Felbamate
- Generic name
- Felbamate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Suspension
- Route
- Oral
- Marketing category
- ANDA · ANDA206314
- Marketed since
- June 16, 2017
- Listing expires
- December 31, 2027
- Pharmacologic class
- Anti-epileptic Agent
Active ingredients
- Felbamate 600 mg/5mL
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 51672-4172-1 | 237 mL in 1 BOTTLE (51672-4172-1) | Jun 16, 2017 |
| 51672-4172-9 | 473 mL in 1 BOTTLE (51672-4172-9) | Jun 16, 2017 |
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