GABAPENTIN
- Product NDC
- 55700-453
- 11-digit product format
- 557000453
- Labeler code
- 55700
- Product ID
- 55700-453_53f1a783-769c-446f-b64e-7d9f699d22b3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GABAPENTIN
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA090705
- Marketing category
- ANDA
- Marketing start
- 2016-06-29
- Marketing end
- 0000-00-00
- Substance
- GABAPENTIN
- Active strength
- 400 mg/1
- Pharmacologic classes
- Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-453-30 | 55700045330 | 30 CAPSULE in 1 BOTTLE (55700-453-30) | 30 capsule | 2016-11-11 | 0000-00-00 | No | No | Current |
| 55700-453-60 | 55700045360 | 60 CAPSULE in 1 BOTTLE (55700-453-60) | 60 capsule | 2016-11-11 | 0000-00-00 | No | No | Current |
| 55700-453-90 | 55700045390 | 90 CAPSULE in 1 BOTTLE (55700-453-90) | 90 capsule | 2016-11-11 | 0000-00-00 | No | No | Current |