Primidone
- Product NDC
- 0603-5371
- 11-digit product format
- 006035371
- Labeler code
- 0603
- Product ID
- 0603-5371_1c33caad-ce65-4bde-a5cd-cada812bfbc5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- primidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Par Pharmaceutical
- Application
- ANDA040586
- Marketing category
- ANDA
- Marketing start
- 2005-02-24
- Marketing end
- 2021-10-31
- 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 |
|---|
| 0603-5371-21 | 00603537121 | 100 TABLET in 1 BOTTLE, PLASTIC (0603-5371-21) | 100 tablet | 2005-02-24 | 2021-09-30 | No | No | Current |
| 0603-5371-28 | 00603537128 | 500 TABLET in 1 BOTTLE, PLASTIC (0603-5371-28) | 500 tablet | 2005-02-24 | 2021-10-31 | No | No | Current |