Gabapentin
- Product NDC
- 50090-4445
- 11-digit product format
- 500904445
- Labeler code
- 50090
- Product ID
- 50090-4445_6dfcd3f7-3a90-4909-aa43-8872871cdff1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA207057
- Marketing category
- ANDA
- Marketing start
- 2019-05-01
- Marketing end
- 0000-00-00
- Substance
- GABAPENTIN
- Active strength
- 600 mg/1
- Pharmacologic classes
- Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-4445 | GABAPENTIN TABLET, COATED [A-S MEDICATION SOLUTIONS] | 6 | Legacy NDC | 20230415_af076d4c-9bdc-4bea-ad13-62800aea9f74.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4445-0 | 50090444500 | 90 TABLET, COATED in 1 BOTTLE (50090-4445-0) | 2019-08-01 | 0000-00-00 | No | No | Current |
| 50090-4445-1 | 50090444501 | 60 TABLET, COATED in 1 BOTTLE (50090-4445-1) | 2019-08-01 | 0000-00-00 | No | No | Current |
| 50090-4445-2 | 50090444502 | 30 TABLET, COATED in 1 BOTTLE (50090-4445-2) | 2019-08-01 | 0000-00-00 | No | No | Current |