Gabapentin
- Product NDC
- 55695-017
- 11-digit product format
- 556950017
- Labeler code
- 55695
- Product ID
- 55695-017_2b876f1a-499b-0abe-e054-00144ff8d46c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Department of State Health Services, Pharmacy Branch
- Application
- ANDA075350
- Marketing category
- ANDA
- Marketing start
- 2010-01-23
- 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 |
|---|
| 55695-017-00 | Gabapentin | 100 in 1 BOTTLE | CAPSULE | 100 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55695-017 | GABAPENTIN CAPSULE [DEPARTMENT OF STATE HEALTH SERVICES, PHARMACY BRANCH] | 1 | Legacy NDC, 1 package rows | 20160311_2b876f1a-49d5-0abe-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 55695-017-00 | 55695001700 | 100 in 1 BOTTLE | Historical |