NDC 67296-2299
Gabapentin 300 mg capsule
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Northstar Rx LLC.'s NDC 16714-662.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Tirupati, India | Makes it and tests it | Problems found, fixed voluntarilyDec 17, 2025 · 5 inspections |
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Repackaging site
- RedPharm Drug, Eden Prairie, MN, United States · repackages it
Recalls
- Oct 17, 2014 · Class II · Aurobindo Pharma USA Inc
Failed Tablet/Capsule Specifications: Complaints of empty capsules received.
Lots: Lot #: GESB14011-A, Exp 12/15
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Gabapentin: every company that makes it
- Form
- capsule, oral
- Strength
- 300 mg
- Approval
- ANDA ANDA078787
- On the market since
- Jan 31, 2008
- Package NDCs
67296-2299-467296-2299-6- Official label
- DailyMed (National Library of Medicine), updated Oct 2, 2026
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