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Dexamethasone
Dexamethasone - 49884-084-01 - (dexamethasone)
Drug Information of Dexamethasone
| Product NDC: | 49884-084 |
| Proprietary Name: | Dexamethasone |
| Non Proprietary Name: | dexamethasone |
| Active Ingredient(s): | .5 mg/1 & nbsp; dexamethasone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dexamethasone
| Product NDC: | 49884-084 |
| Labeler Name: | Par Pharmaceutical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA088148 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19830428 |
Package Information of Dexamethasone
| Package NDC: | 49884-084-01 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (49884-084-01) |
NDC Information of Dexamethasone
| NDC Code | 49884-084-01 |
| Proprietary Name | Dexamethasone |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (49884-084-01) |
| Product NDC | 49884-084 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | dexamethasone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19830428 |
| Marketing Category Name | ANDA |
| Labeler Name | Par Pharmaceutical Inc. |
| Substance Name | DEXAMETHASONE |
| Strength Number | .5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
