NDC 71205-514 – Gabapentin
Gabapentin 800 mg/1 · Tablet · Oral
Product NDC71205-514
Product details
- Brand name
- Gabapentin
- Generic name
- Gabapentin
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA205101
- Marketed since
- February 4, 2016
- Listing expires
- December 31, 2026
- Pharmacologic class
- Anti-epileptic Agent
Active ingredients
- Gabapentin 800 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 71205-514-30 | 30 TABLET in 1 BOTTLE (71205-514-30) | Dec 9, 2020 |
| 71205-514-60 | 60 TABLET in 1 BOTTLE (71205-514-60) | Dec 9, 2020 |
| 71205-514-90 | 90 TABLET in 1 BOTTLE (71205-514-90) | Dec 9, 2020 |
Other Gabapentin products
- 50090-7715 Gabapentin 600 mg/1 · Tablet · A-S Medication Solutions
- 50090-7714 Gabapentin 600 mg/1 · Tablet · A-S Medication Solutions
- 50090-6189 Gabapentin 800 mg/1 · Tablet · A-S Medication Solutions
- 72888-132 Gabapentin 800 mg/1 · Tablet · Advagen Pharma Ltd
- 72888-131 Gabapentin 600 mg/1 · Tablet · Advagen Pharma Ltd
- 80425-0035 Gabapentin 800 mg/1 · Tablet · Advanced Rx of Tennessee, LLC
- 71610-630 Gabapentin 800 mg/1 · Tablet · Aphena Pharma Solutions - Tennessee, LLC
- 71610-737 Gabapentin 800 mg/1 · Tablet · Aphena Pharma Solutions - Tennessee, LLC
- 71610-777 Gabapentin 600 mg/1 · Tablet · Aphena Pharma Solutions - Tennessee, LLC
- 71610-767 Gabapentin 600 mg/1 · Tablet · Aphena Pharma Solutions - Tennessee, LLC
- 71610-778 Gabapentin 800 mg/1 · Tablet · Aphena Pharma Solutions - Tennessee, LLC
- 71610-621 Gabapentin 600 mg/1 · Tablet · Aphena Pharma Solutions - Tennessee, LLC