Gabapentin
- Product NDC
- 60760-939
- 11-digit product format
- 607600939
- Labeler code
- 60760
- Product ID
- 60760-939_4a65ae80-91dd-a433-e063-6294a90a055c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- Application
- ANDA206943
- Marketing category
- ANDA
- Marketing start
- 2025-01-08
- Substance
- GABAPENTIN
- Active strength
- 100 mg/1
- Pharmacologic classes
- Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Gabapentin
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| GABAPENTIN | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6CW7F3G59X |
| Rxcui | 310430 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60760-939-60 | Gabapentin | 60 in 1 BOTTLE, PLASTIC | CAPSULE | 60 | | 3 |
| 60760-939-90 | Gabapentin | 90 in 1 BOTTLE, PLASTIC | CAPSULE | 90 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 60760-939-60 | 60760093960 | 60 CAPSULE in 1 BOTTLE, PLASTIC (60760-939-60) | 60 capsule | 2025-08-14 | No | No | Current |
| 60760-939-90 | 60760093990 | 90 CAPSULE in 1 BOTTLE, PLASTIC (60760-939-90) | 90 capsule | 2026-02-04 | No | No | Current |