Details for New Drug Application (NDA): 072041
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NDA 072041 describes DERMABET, which is a drug marketed by Sun Pharma Canada and is included in one NDA. It is available from four suppliers. Additional details are available on the DERMABET profile page.
The generic ingredient in DERMABET is betamethasone valerate. There are sixty-six drug master file entries for this compound. Fourteen suppliers are listed for this compound. Additional details are available on the betamethasone valerate profile page.
The generic ingredient in DERMABET is betamethasone valerate. There are sixty-six drug master file entries for this compound. Fourteen suppliers are listed for this compound. Additional details are available on the betamethasone valerate profile page.
Summary for 072041
| Tradename: | DERMABET |
| Applicant: | Sun Pharma Canada |
| Ingredient: | betamethasone valerate |
| Patents: | 0 |
Pharmacology for NDA: 072041
| Mechanism of Action | Corticosteroid Hormone Receptor Agonists |
Medical Subject Heading (MeSH) Categories for 072041
Suppliers and Packaging for NDA: 072041
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| DERMABET | betamethasone valerate | CREAM;TOPICAL | 072041 | ANDA | A-S Medication Solutions | 50090-1647 | 50090-1647-0 | 1 TUBE in 1 CARTON (50090-1647-0) / 15 g in 1 TUBE |
| DERMABET | betamethasone valerate | CREAM;TOPICAL | 072041 | ANDA | A-S Medication Solutions | 50090-3134 | 50090-3134-1 | 1 TUBE in 1 CARTON (50090-3134-1) / 45 g in 1 TUBE |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | CREAM;TOPICAL | Strength | EQ 0.1% BASE | ||||
| Approval Date: | Jan 6, 1988 | TE: | AB | RLD: | No | ||||
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