Dexamethasone
- Product NDC
- 0095-0089
- 11-digit product format
- 000950089
- Labeler code
- 0095
- Product ID
- 0095-0089_917738ba-3e5c-4ef1-9bd8-13be8b393cb8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dexamethasone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bausch Health US LLC
- Application
- ANDA040700
- Marketing category
- ANDA
- Marketing start
- 2009-04-01
- Marketing end
- 0000-00-00
- Substance
- DEXAMETHASONE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 0095-0089-21 | 00095008921 | 21 TABLET in 1 BLISTER PACK (0095-0089-21) | 21 tablet | 2009-04-01 | 0000-00-00 | No | No | Current |