Gabapentin
- Product NDC
- 66116-358
- 11-digit product format
- 661160358
- Labeler code
- 66116
- Product ID
- 66116-358_6b3ca748-7172-4c53-b5ae-7e17dad918eb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- MedVantx, Inc.
- Application
- ANDA075350
- Marketing category
- ANDA
- Marketing start
- 2004-10-04
- 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
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 66116-358-60 | Gabapentin | 60 in 1 BOTTLE | CAPSULE | 60 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 66116-358 | GABAPENTIN CAPSULE [MEDVANTX, INC.] | 1 | Legacy NDC, 1 package rows | 20111220_6b3ca748-7172-4c53-b5ae-7e17dad918eb.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 66116-358-60 | 66116035860 | 60 in 1 BOTTLE | Historical |