Primidone
- Product NDC
- 50090-4083
- 11-digit product format
- 500904083
- Labeler code
- 50090
- Product ID
- 50090-4083_b3175649-c6a8-47ab-8adc-d84885b13274
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Primidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040866
- Marketing category
- ANDA
- Marketing start
- 2009-12-24
- Marketing end
- 0000-00-00
- Substance
- PRIMIDONE
- Active strength
- 250 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#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4083-0 | 50090408300 | 100 TABLET in 1 BOTTLE (50090-4083-0) | 100 tablet | 2019-01-24 | 0000-00-00 | No | No | Current |