Gabapentin
- Product NDC
- 67296-1709
- 11-digit product format
- 672961709
- Labeler code
- 67296
- Product ID
- 67296-1709_b8dfb538-7988-5311-e053-2995a90a07bd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA206943
- Marketing category
- ANDA
- Marketing start
- 2018-05-14
- 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 |
|---|
| 67296-1709-3 | Gabapentin | 30 in 1 BOTTLE | CAPSULE | 30 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1709 | GABAPENTIN CAPSULE [REDPHARM DRUG, INC.] | 7 | Legacy NDC, 1 package rows | 20210115_96cb7daa-a57a-6b0b-e053-2995a90add23.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 |
|---|
| 67296-1709-3 | 67296170903 | 30 CAPSULE in 1 BOTTLE (67296-1709-3) | 30 capsule | 2019-11-01 | 0000-00-00 | No | No | Current |