NDC 47335-691 – Pregabalin
Pregabalin 200 mg/1 · Capsule · Oral
Product NDC47335-691
Product details
- Brand name
- Pregabalin
- Generic name
- Pregabalin
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA091157
- Marketed since
- December 4, 2019
- Listing expires
- December 31, 2026
Active ingredients
- Pregabalin 200 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 47335-691-08 | 100 CAPSULE in 1 BOTTLE (47335-691-08) | Dec 4, 2019 |
| 47335-691-18 | 1000 CAPSULE in 1 BOTTLE (47335-691-18) | Dec 4, 2019 |
| 47335-691-83 | 30 CAPSULE in 1 BOTTLE (47335-691-83) | Dec 4, 2019 |
| 47335-691-88 | 100 CAPSULE in 1 BOTTLE (47335-691-88) | Dec 4, 2019 |
Recalls mentioning this NDC
- D-0361-2022 Jan 12, 2022 · Class II
Failed Tablet/Capsule Specifications: Out of Specification results for particle Size Distribution and Bulk Density of the Active Pharmaceutical Ingredient.
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