Diazepam 70518-1713
Product NDC
70518-1713- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- December 6, 2018
- Listing Expires
- December 31, 2027
- Application
- ANDA071321
Active Ingredients
| Ingredient | Strength |
|---|---|
| Diazepam | 5 mg/1 |
Drug Class
Benzodiazepine [EPC]Benzodiazepine [EPC]Benzodiazepines [CS]
Packaging Options(2)
30 TABLET in 1 BLISTER PACK (70518-1713-0)
100 POUCH in 1 BOX, UNIT-DOSE (70518-1713-4) / 1 TABLET in 1 POUCH (70518-1713-5)