Gabapentin
- Product NDC
- 50090-5125
- 11-digit product format
- 500905125
- Labeler code
- 50090
- Product ID
- 50090-5125_10e44c2d-0068-4893-8931-82e9253adba8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090858
- Marketing category
- ANDA
- Marketing start
- 2011-01-29
- 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
- 2022-12-31
- 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 |
|---|
| 50090-5125-0 | Gabapentin | 1 in 1 BLISTER PACK | CAPSULE | 1 | | 3 |
| 50090-5125-0 | Gabapentin | 33 in 1 BOX, UNIT-DOSE | CAPSULE | 33 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5125 | GABAPENTIN CAPSULE [A-S MEDICATION SOLUTIONS] | 3 | Legacy NDC, 2 package rows | 20210416_eb3ac1fa-d7ac-476f-973a-a36258e2db74.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5125-0 | 50090512500 | 33 BLISTER PACK in 1 BOX, UNIT-DOSE (50090-5125-0) > 1 CAPSULE in 1 BLISTER PACK | 33 blister pack | 2020-08-07 | 0000-00-00 | No | No | Current |