Gabapentin
- Product NDC
- 50090-2561
- 11-digit product format
- 500902561
- Labeler code
- 50090
- Product ID
- 50090-2561_7d001229-8d8a-4afe-892b-66ec8f36efad
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075350
- Marketing category
- ANDA
- Marketing start
- 2014-04-23
- Marketing end
- 0000-00-00
- Substance
- GABAPENTIN
- Active strength
- 100 mg/1
- Pharmacologic classes
- Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-2561-0 | Gabapentin | 30 in 1 BOTTLE | CAPSULE | 30 | | 6 |
| 50090-2561-1 | Gabapentin | 100 in 1 BOTTLE | CAPSULE | 100 | | 6 |
| 50090-2561-2 | Gabapentin | 90 in 1 BOTTLE | CAPSULE | 90 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2561 | GABAPENTIN CAPSULE [A-S MEDICATION SOLUTIONS] | 6 | Legacy NDC, 3 package rows | 20190225_57a431ef-982d-4d5a-9bf2-e07da192bff7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50090-2561-0 | 50090256100 | 30 in 1 BOTTLE | Historical |
| 50090-2561-1 | 50090256101 | 100 in 1 BOTTLE | Historical |
| 50090-2561-2 | 50090256102 | 90 in 1 BOTTLE | Historical |