Gabapentin
- Product NDC
- 50090-3318
- 11-digit product format
- 500903318
- Labeler code
- 50090
- Product ID
- 50090-3318_421d9dd5-0cbd-403f-b79a-29215f48359c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075350
- Marketing category
- ANDA
- Marketing start
- 2014-04-03
- Marketing end
- 0000-00-00
- Substance
- GABAPENTIN
- Active strength
- 300 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 |
|---|
| 50090-3318-0 | Gabapentin | 33 in 1 BOX, UNIT-DOSE | CAPSULE | 33 | | 7 |
| 50090-3318-0 | Gabapentin | 1 in 1 BLISTER PACK | CAPSULE | 1 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3318 | GABAPENTIN CAPSULE [A-S MEDICATION SOLUTIONS] | 7 | Legacy NDC, 2 package rows | 20180820_e31879cd-2fd8-4057-b43e-bbb9f307b761.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50090-3318-0 | 50090331800 | 33 in 1 BOX, UNIT-DOSE | Historical |