Gabapentin
- Product NDC
- 50436-0224
- 11-digit product format
- 504360224
- Labeler code
- 50436
- Product ID
- 50436-0224_2ea50626-b62d-459a-9c39-bd3da454afda
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA090858
- Marketing category
- ANDA
- Marketing start
- 2011-01-29
- 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
- 2023-12-31
- 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 |
|---|
| 50436-0224-2 | Gabapentin | 60 in 1 BOTTLE | CAPSULE | 60 | | 13 |
| 50436-0224-3 | Gabapentin | 90 in 1 BOTTLE | CAPSULE | 90 | | 13 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-0224 | GABAPENTIN CAPSULE [UNIT DOSE SERVICES] | 13 | Legacy NDC, 2 package rows | 20221117_517fdc6d-5e72-4ee6-8471-7a7f8f4ecfe7.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 |
|---|
| 50436-0224-2 | 50436022402 | 60 CAPSULE in 1 BOTTLE (50436-0224-2) | 60 capsule | 2016-08-01 | 0000-00-00 | No | No | Current |
| 50436-0224-3 | 50436022403 | 90 CAPSULE in 1 BOTTLE (50436-0224-3) | 90 capsule | 2016-08-01 | 0000-00-00 | No | No | Current |