RILUZOLE
- Product NDC
- 60505-3285
- 11-digit product format
- 605053285
- Labeler code
- 60505
- Product ID
- 60505-3285_f26808ab-9402-1018-b397-fd176c9b8c67
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- RILUZOLE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Apotex Corp
- Application
- ANDA091300
- Marketing category
- ANDA
- Marketing start
- 2013-06-18
- Marketing end
- 2021-10-31
- Substance
- RILUZOLE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Benzothiazole [EPC],Benzothiazoles [CS]
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60505-3285-6 | 60505328506 | 60 TABLET, FILM COATED in 1 BOTTLE (60505-3285-6) | 2013-06-18 | 2021-10-31 | No | No | Current |