NDC 0904-6665 – Gabapentin
Gabapentin 100 mg/1 · Capsule · Oral
Product NDC0904-6665
Product details
- Brand name
- Gabapentin
- Generic name
- Gabapentin
- Labeler
- Major Pharmaceuticals
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA090858
- Marketed since
- January 29, 2011
- Marketing end
- April 30, 2027
Active ingredients
- Gabapentin 100 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0904-6665-61 | 100 BLISTER PACK in 1 CARTON (0904-6665-61) / 1 CAPSULE in 1 BLISTER PACK | Jan 29, 2011 |
Recalls mentioning this NDC
- D-0030-2026 Oct 29, 2025 · Class II
Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity . - D-0031-2026 Oct 29, 2025 · Class II
Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity . - D-0507-2025 Jul 9, 2025 · Class II
Defective container; blister packaging inadequately sealed.
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