Estazolam
- Product NDC
- 51862-070
- 11-digit product format
- 518620070
- Labeler code
- 51862
- Product ID
- 51862-070_7e901c43-dae9-45fe-a498-0493fe441ab8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Estazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mayne Pharma
- Application
- ANDA074921
- Marketing category
- ANDA
- Marketing start
- 2016-08-03
- Marketing end
- 2022-05-31
- Substance
- ESTAZOLAM
- Active strength
- 2 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- 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 |
|---|
| 51862-070-01 | 51862007001 | 100 TABLET in 1 BOTTLE (51862-070-01) | 100 tablet | 2016-08-03 | 2022-05-31 | No | No | Current |