Betamethasone Sodium Phosphate and Betamethasone Acetate (PharmaForce, Inc.)
Welcome to the PulseAid listing for the Betamethasone Sodium Phosphate and Betamethasone Acetate drug offered from PharmaForce, 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: | PharmaForce, 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: | 2009-07-31 |
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 PharmaForce, Inc. |
LABELER NAME: | PharmaForce, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 3; 3(mg/mL; mg/mL) |
START MARKETING DATE: | 2009-07-31 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 40042-048_f8cfe50b-e269-47f2-8ce6-0b40511945bc |
PRODUCT NDC: | 40042-048 |
APPLICATION NUMBER: | ANDA090747 |
Other BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE Pharmaceutical Manufacturers / Labelers: