Gabapentin
- Product NDC
- 63739-903
- 11-digit product format
- 637390903
- Labeler code
- 63739
- Product ID
- 63739-903_159496fe-700e-4c94-a766-7809a7ce1839
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- McKesson Corporation dba Sky Packaging
- Application
- ANDA090858
- Marketing category
- ANDA
- Marketing start
- 2021-07-15
- Substance
- GABAPENTIN
- Active strength
- 300 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 | 300 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6CW7F3G59X |
| Rxcui | 310430, 310431, 310432 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63739-903-10 | Gabapentin | 10 in 1 BLISTER PACK | CAPSULE | 10 | | 4 |
| 63739-903-10 | Gabapentin | 10 in 1 CARTON | CAPSULE | 10 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63739-903 | GABAPENTIN CAPSULE [MCKESSON CORPORATION DBA SKY PACKAGING] | 4 | Current NDC, Legacy NDC, 2 package rows | 20250418_23eb133e-2f74-4219-9892-0a8e770ec032.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 |
|---|
| 63739-903-10 | 63739090310 | 10 BLISTER PACK in 1 CARTON (63739-903-10) / 10 CAPSULE in 1 BLISTER PACK | 10 blister pack | 2021-07-15 | 0000-00-00 | No | No | Current |