Dexamethasone
- Product NDC
- 48102-046
- 11-digit product format
- 481020046
- Labeler code
- 48102
- Product ID
- 48102-046_cac182c0-8f23-49c4-8941-2732616e1b35
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dexamethasone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Fera Pharmaceuticals, LLC
- Application
- ANDA088481
- Marketing category
- ANDA
- Marketing start
- 2018-06-01
- Marketing end
- 0000-00-00
- Substance
- DEXAMETHASONE
- Active strength
- 1 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 |
|---|
| 48102-046-01 | 48102004601 | 100 TABLET in 1 BOTTLE (48102-046-01) | 100 tablet | 2018-06-01 | 0000-00-00 | No | No | Current |