Gabapentin
- Product NDC
- 55695-016
- 11-digit product format
- 556950016
- Labeler code
- 55695
- Product ID
- 55695-016_2b87248b-66e7-70ac-e054-00144ff8d46c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Department of State Health Services, Pharmacy Branch
- Application
- ANDA090858
- Marketing category
- ANDA
- Marketing start
- 2011-01-29
- 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
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 55695-016-00 | 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 |
|---|
| 55695-016 | GABAPENTIN CAPSULE [DEPARTMENT OF STATE HEALTH SERVICES, PHARMACY BRANCH] | 1 | Legacy NDC, 1 package rows | 20160311_2b87248b-6703-70ac-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 55695-016-00 | 55695001600 | 100 in 1 BOTTLE | Historical |