NDC 62756-202 – Gabapentin
Gabapentin 600 mg/1 · Tablet, Film Coated · Oral
Product NDC62756-202
Product details
- Brand name
- Gabapentin
- Generic name
- Gabapentin
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077525
- Marketed since
- September 1, 2022
- Listing expires
- December 31, 2027
Active ingredients
- Gabapentin 600 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 62756-202-01 | 100 TABLET, FILM COATED in 1 BOTTLE (62756-202-01) | Sep 1, 2022 |
| 62756-202-03 | 500 TABLET, FILM COATED in 1 BOTTLE (62756-202-03) | Sep 1, 2022 |
Recalls mentioning this NDC
- D-0311-2025 Apr 16, 2025 · Class III
Cross Contamination - D-0312-2025 Apr 16, 2025 · Class III
Cross Contamination
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