Details for New Drug Application (NDA): 205932
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The generic ingredient in PITAVASTATIN CALCIUM is pitavastatin calcium. There are fifteen drug master file entries for this compound. Ten suppliers are listed for this compound. Additional details are available on the pitavastatin calcium profile page.
Summary for 205932
Tradename: | PITAVASTATIN CALCIUM |
Applicant: | Orient Pharma Co Ltd |
Ingredient: | pitavastatin calcium |
Patents: | 0 |
Pharmacology for NDA: 205932
Mechanism of Action | Hydroxymethylglutaryl-CoA Reductase Inhibitors |
Suppliers and Packaging for NDA: 205932
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
PITAVASTATIN CALCIUM | pitavastatin calcium | TABLET;ORAL | 205932 | ANDA | Teva Pharmaceuticals, Inc. | 0480-3631 | 0480-3631-98 | 90 TABLET, FILM COATED in 1 BOTTLE (0480-3631-98) |
PITAVASTATIN CALCIUM | pitavastatin calcium | TABLET;ORAL | 205932 | ANDA | Teva Pharmaceuticals, Inc. | 0480-3632 | 0480-3632-98 | 90 TABLET, FILM COATED in 1 BOTTLE (0480-3632-98) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 1MG BASE | ||||
Approval Date: | Feb 3, 2017 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 2MG BASE | ||||
Approval Date: | Feb 3, 2017 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 4MG BASE | ||||
Approval Date: | Feb 3, 2017 | TE: | AB | RLD: | No |
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