Alprazolam
- Product NDC
- 55700-671
- 11-digit product format
- 557000671
- Labeler code
- 55700
- Product ID
- 55700-671_af7393d2-1a1a-4524-8f40-38476dc4dfc4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA074174
- Marketing category
- ANDA
- Marketing start
- 2018-08-24
- Marketing end
- 0000-00-00
- Substance
- ALPRAZOLAM
- Active strength
- 0 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-671-30 | 55700067130 | 30 TABLET in 1 BOTTLE (55700-671-30) | 30 tablet | 2018-08-24 | 0000-00-00 | No | No | Current |
| 55700-671-60 | 55700067160 | 60 TABLET in 1 BOTTLE (55700-671-60) | 60 tablet | 2018-08-24 | 0000-00-00 | No | No | Current |