Gabapentin
- Product NDC
- 52343-031
- 11-digit product format
- 523430031
- Labeler code
- 52343
- Product ID
- 52343-031_19e835f7-2223-4d65-a702-70176cd1c9c7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- ACETRIS HEALTH, LLC
- Application
- ANDA078787
- Marketing category
- ANDA
- Marketing start
- 2008-01-31
- Marketing end
- 2020-09-01
- Substance
- GABAPENTIN
- Active strength
- 300 mg/1
- Pharmacologic classes
- Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 52343-031-01 | EA - Each | 52343-031 | 93eb33d7-d80c-4f27-8a75-9896ffeb3588 | 1 | 2013-08-02 |
| 52343-031-18 | EA - Each | 52343-031 | 6b1bdcf5-75e6-4c64-a9bd-44ac01905d93 | 1 | 2013-08-02 |
| 52343-031-27 | EA - Each | 52343-031 | 4024ed79-4082-4123-911b-3eb4ce8d00ef | 1 | 2013-08-02 |
| 52343-031-30 | EA - Each | 52343-031 | e4b27f81-68c3-4ebd-9b73-fc3e28a91291 | 1 | 2013-08-02 |
| 52343-031-60 | EA - Each | 52343-031 | 33992381-3cc7-4b95-b85e-7aeaed17f644 | 1 | 2013-08-02 |
| 52343-031-90 | EA - Each | 52343-031 | 4bafe2f4-c5de-4241-9cd0-4e1160fe72c1 | 1 | 2013-08-02 |
| 52343-031-99 | EA - Each | 52343-031 | a21c7f8c-8e9f-4f85-b12f-53bcb7ba96cf | 1 | 2013-08-02 |