Dexamethasone
- Product NDC
- 42195-151
- 11-digit product format
- 421950151
- Labeler code
- 42195
- Product ID
- 42195-151_ca5ee247-a436-42b8-a4a5-388946e6c8e2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DEXAMETHASONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Xspire Pharma, LLC
- Application
- ANDA088237
- Marketing category
- ANDA
- Marketing start
- 2019-01-04
- 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
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 |
|---|
| 42195-151-10 | 42195015110 | 100 TABLET in 1 BOTTLE (42195-151-10) | 100 tablet | 2019-01-04 | 0000-00-00 | No | No | Current |