Primidone
- Product NDC
- 0904-5559
- 11-digit product format
- 009045559
- Labeler code
- 0904
- Product ID
- 0904-5559_33874435-eb52-4f58-a02a-a28d88658cd5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Primidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA084903
- Marketing category
- ANDA
- Marketing start
- 2005-04-07
- Marketing end
- 2022-04-30
- Substance
- PRIMIDONE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-5559-60 | 00904555960 | 100 TABLET in 1 BOTTLE (0904-5559-60) | 100 tablet | 2005-04-07 | 2022-04-30 | No | No | Current |