Details for New Drug Application (NDA): 207408
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The generic ingredient in ROSUVASTATIN CALCIUM is rosuvastatin calcium. There are forty-two drug master file entries for this compound. Forty-five suppliers are listed for this compound. Additional details are available on the rosuvastatin calcium profile page.
Summary for 207408
| Tradename: | ROSUVASTATIN CALCIUM |
| Applicant: | Changzhou Pharm |
| Ingredient: | rosuvastatin calcium |
| Patents: | 0 |
Pharmacology for NDA: 207408
| Mechanism of Action | Hydroxymethylglutaryl-CoA Reductase Inhibitors |
Medical Subject Heading (MeSH) Categories for 207408
Suppliers and Packaging for NDA: 207408
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| ROSUVASTATIN CALCIUM | rosuvastatin calcium | TABLET;ORAL | 207408 | ANDA | Cranbury Pharmaceuticals, LLC | 27808-155 | 27808-155-01 | 90 TABLET, FILM COATED in 1 BOTTLE (27808-155-01) |
| ROSUVASTATIN CALCIUM | rosuvastatin calcium | TABLET;ORAL | 207408 | ANDA | Cranbury Pharmaceuticals, LLC | 27808-155 | 27808-155-02 | 1000 TABLET, FILM COATED in 1 BOTTLE (27808-155-02) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 5MG BASE | ||||
| Approval Date: | Oct 31, 2016 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 10MG BASE | ||||
| Approval Date: | Oct 31, 2016 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 20MG BASE | ||||
| Approval Date: | Oct 31, 2016 | TE: | AB | RLD: | No | ||||
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