Betamethasone Sodium Phosphate and Betamethasone Acetate (American Regent, Inc.)
Welcome to the PulseAid listing for the Betamethasone Sodium Phosphate and Betamethasone Acetate drug offered from American Regent, Inc.. This Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
| LABELER NAME / MANUFACTURER: | American Regent, Inc. |
| NON-PROPRIETARY NAME: | Betamethasone Sodium Phosphate and Betamethasone Acetate |
| SUBSTANCE NAME: | BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
| ROUTE: | INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR |
| DOSAGE FORM: | INJECTION, SUSPENSION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2010-04-28 |
| END MARKETING DATE: | 0000-00-00 |
Betamethasone Sodium Phosphate and Betamethasone Acetate HUMAN PRESCRIPTION DRUG Details:
| Item Description | Betamethasone Sodium Phosphate and Betamethasone Acetate from American Regent, Inc. |
| LABELER NAME: | American Regent, Inc. |
| DEA SCHEDULE: |
|
| ACTIVE STRENGTH: | 3; 3(mg/mL; mg/mL) |
| START MARKETING DATE: | 2010-04-28 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0517-0720_0deadaca-96c5-4759-ae1f-d76b44120507 |
| PRODUCT NDC: | 0517-0720 |
| APPLICATION NUMBER: | ANDA090747 |
Other BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE Pharmaceutical Manufacturers / Labelers:
