Estazolam
- Product NDC
- 51862-073
- 11-digit product format
- 518620073
- Labeler code
- 51862
- Product ID
- 51862-073_fc2d4f1d-8898-4fa8-858e-59d60daca9e0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Estazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mayne Pharma
- Application
- ANDA074921
- Marketing category
- ANDA
- Marketing start
- 2020-10-18
- Marketing end
- 0000-00-00
- Substance
- ESTAZOLAM
- Active strength
- 1 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- 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 |
|---|
| 51862-073-01 | 51862007301 | 100 TABLET in 1 BOTTLE, PLASTIC (51862-073-01) | 100 tablet | 2020-10-18 | 0000-00-00 | No | No | Current |