Gabapentin
- Product NDC
- 50090-2107
- 11-digit product format
- 500902107
- Labeler code
- 50090
- Product ID
- 50090-2107_c70e6adb-6edc-48d6-8af5-6a1d42feb7ae
- 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
- 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#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-2107-0 | Gabapentin | 90 in 1 BOTTLE | CAPSULE | 90 | | 44 |
| 50090-2107-1 | Gabapentin | 30 in 1 BOTTLE | CAPSULE | 30 | | 44 |
| 50090-2107-2 | Gabapentin | 60 in 1 BOTTLE | CAPSULE | 60 | | 44 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2107 | GABAPENTIN CAPSULE [A-S MEDICATION SOLUTIONS] | 40 | Legacy NDC, 3 package rows | 20250417_03031adf-d36b-45ec-944e-dfce5a5de91a.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 |
|---|
| 50090-2107-0 | 50090210700 | 90 CAPSULE in 1 BOTTLE (50090-2107-0) | 90 capsule | 2015-10-14 | 0000-00-00 | No | No | Current |
| 50090-2107-1 | 50090210701 | 30 CAPSULE in 1 BOTTLE (50090-2107-1) | 30 capsule | 2018-07-27 | 0000-00-00 | No | No | Current |
| 50090-2107-2 | 50090210702 | 60 in 1 BOTTLE | | | | | | Historical |