Gabapentin
- Product NDC
- 82804-226
- 11-digit product format
- 828040226
- Labeler code
- 82804
- Product ID
- 82804-226_9d401e54-d4f5-43ba-b898-dd08fc3c7bfa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA075477
- Marketing category
- ANDA
- Marketing start
- 2021-11-01
- Substance
- GABAPENTIN
- Active strength
- 100 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 | 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 |
|---|
| 82804-226-30 | Gabapentin | 30 in 1 BOTTLE, PLASTIC | CAPSULE | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 82804-226 | GABAPENTIN CAPSULE [PROFICIENT RX LP] | 1 | Current NDC, 1 package rows | 20250529_9d401e54-d4f5-43ba-b898-dd08fc3c7bfa.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 |
|---|
| 82804-226-30 | 82804022630 | 30 CAPSULE in 1 BOTTLE, PLASTIC (82804-226-30) | 30 capsule | 2025-05-23 | No | No | Current |