NDC 43598-296 – pregabalin
Pregabalin 200 mg/1 · Capsule · Oral
Product NDC43598-296
Product details
- Brand name
- pregabalin
- Generic name
- pregabalin
- Labeler
- Dr.Reddys Laboratories Inc
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA209664
- Marketed since
- July 19, 2019
- Listing expires
- December 31, 2026
Active ingredients
- Pregabalin 200 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 43598-296-05 | 500 CAPSULE in 1 BOTTLE (43598-296-05) | Jul 19, 2019 |
| 43598-296-66 | 5 BLISTER PACK in 1 CARTON (43598-296-66) / 10 CAPSULE in 1 BLISTER PACK (43598-296-79) | Jul 19, 2019 |
| 43598-296-78 | 10 BLISTER PACK in 1 CARTON (43598-296-78) / 10 CAPSULE in 1 BLISTER PACK (43598-296-79) | Jul 19, 2019 |
| 43598-296-90 | 90 CAPSULE in 1 BOTTLE (43598-296-90) | Jul 19, 2019 |
Recalls mentioning this NDC
- D-0469-2021 Jun 2, 2021 · Class II
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
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