NDC 71205-160 – Gabapentin
Gabapentin 800 mg/1 · Tablet, Film Coated · Oral
Product NDC71205-160
Product details
- Brand name
- Gabapentin
- Generic name
- Gabapentin
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA203244
- Marketed since
- January 11, 2014
- Listing expires
- December 31, 2026
- Pharmacologic class
- Anti-epileptic Agent
Active ingredients
- Gabapentin 800 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 71205-160-30 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-160-30) | Nov 1, 2018 |
| 71205-160-60 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-160-60) | Nov 1, 2018 |
| 71205-160-90 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-160-90) | Nov 1, 2018 |
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