Diastat
- Product NDC
- 0187-0659
- 11-digit product format
- 001870659
- Labeler code
- 0187
- Product ID
- 0187-0659_1e7e58ee-24d8-4c34-8e85-7f3a8b425e01
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- diazepam
- Dosage form
- GEL
- Route
- RECTAL
- Labeler
- Bausch Health US, LLC
- Application
- NDA020648
- Marketing category
- NDA
- Marketing start
- 1997-07-29
- Marketing end
- 0000-00-00
- Substance
- DIAZEPAM
- Active strength
- 20 mg/4mL
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 0187-0659-20 | 00187065920 | 2 SYRINGE, PLASTIC in 1 PACKAGE (0187-0659-20) > 4 mL in 1 SYRINGE, PLASTIC | 1997-07-29 | 0000-00-00 | No | No | Current |