Dexamethasone
- Product NDC
- 50090-0089
- 11-digit product format
- 500900089
- Labeler code
- 50090
- Product ID
- 50090-0089_53b8cfb8-9ada-4e16-9fdb-a6a8c00e2d63
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dexamethasone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA084612
- Marketing category
- ANDA
- Marketing start
- 1978-07-19
- Marketing end
- 0000-00-00
- Substance
- DEXAMETHASONE
- Active strength
- 4 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 |
|---|
| 50090-0089-0 | 50090008900 | 28 TABLET in 1 BOTTLE, PLASTIC (50090-0089-0) | 28 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |