Gabapentin
- Product NDC
- 72162-1530
- 11-digit product format
- 721621530
- Labeler code
- 72162
- Product ID
- 72162-1530_e788291e-59d2-4df8-b92d-da8d7c2d8070
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA205101
- Marketing category
- ANDA
- Marketing start
- 2016-02-04
- Substance
- GABAPENTIN
- Active strength
- 600 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 | 600 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6CW7F3G59X |
| Rxcui | 310433 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-1530-1 | Gabapentin | 100 in 1 BOTTLE | TABLET | 100 | | 101 |
| 72162-1530-5 | Gabapentin | 500 in 1 BOTTLE | TABLET | 500 | | 101 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-1530 | GABAPENTIN TABLET [BRYANT RANCH PREPACK] | 100 | Current NDC, 2 package rows | 20240203_56378630-e7a7-4981-8212-8ea703a433d8.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 |
|---|
| 72162-1530-1 | 72162153001 | 100 TABLET in 1 BOTTLE (72162-1530-1) | 100 tablet | 2018-08-20 | No | No | Historical |
| 72162-1530-5 | 72162153005 | 500 TABLET in 1 BOTTLE (72162-1530-5) | 500 tablet | 2018-08-20 | No | No | Historical |