Dexamethasone
- Product NDC
- 48102-051
- 11-digit product format
- 481020051
- Labeler code
- 48102
- Product ID
- 48102-051_9bd5d640-0f1e-4a18-aa47-aea564f46f1f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dexamethasone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Fera Pharmaceuticals, LLC
- Application
- ANDA088481
- Marketing category
- ANDA
- Marketing start
- 2021-06-01
- Marketing end
- 2023-12-31
- Substance
- DEXAMETHASONE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 48102-051-01 | 48102005101 | 100 TABLET in 1 BOTTLE (48102-051-01) | 100 tablet | 2021-06-01 | 0000-00-00 | No | No | Current |
| 48102-051-20 | 48102005120 | 10 BLISTER PACK in 1 CARTON (48102-051-20) > 10 TABLET in 1 BLISTER PACK (48102-051-11) | 10 blister pack | 2021-06-01 | 0000-00-00 | No | No | Current |
| 48102-051-40 | 48102005140 | 40 TABLET in 1 BOTTLE (48102-051-40) | 40 tablet | 2021-06-01 | 0000-00-00 | No | No | Current |