Primidone
- Product NDC
- 68682-691
- 11-digit product format
- 686820691
- Labeler code
- 68682
- Product ID
- 68682-691_ee79cbb9-c8fc-4714-894c-a5d6b5c5dcfd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Primidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Oceanside Pharmaceuticals
- Application
- NDA009170
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2018-05-21
- Marketing end
- 0000-00-00
- 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
- 2020-12-31
- 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 |
|---|
| 68682-691-10 | 68682069110 | 100 TABLET in 1 BOTTLE (68682-691-10) | 100 tablet | 2018-05-21 | 0000-00-00 | No | No | Current |