Gabapentin
- Product NDC
- 72189-619
- 11-digit product format
- 721890619
- Labeler code
- 72189
- Product ID
- 72189-619_3375e0cd-d3ed-64d5-e063-6294a90ac5e5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA206402
- Marketing category
- ANDA
- Marketing start
- 2025-03-18
- Substance
- GABAPENTIN
- Active strength
- 800 mg/1
- Pharmacologic classes
- Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Gabapentin
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| GABAPENTIN | 800 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6CW7F3G59X |
| Rxcui | 310434 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-619-72 | Gabapentin | 120 in 1 BOTTLE | TABLET | 120 | | 2 |
| 72189-619-90 | Gabapentin | 90 in 1 BOTTLE | TABLET | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-619 | GABAPENTIN TABLET [DIRECT_RX] | 2 | Current NDC, 2 package rows | 20250425_30a2ed14-dcda-f972-e063-6294a90a417c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-619-72 | 72189061972 | 120 TABLET in 1 BOTTLE (72189-619-72) | 120 tablet | 2025-03-18 | No | No | Historical |
| 72189-619-90 | 72189061990 | 90 TABLET in 1 BOTTLE (72189-619-90) | 90 tablet | 2025-03-18 | No | No | Historical |