Details for New Drug Application (NDA): 202438
✉ Email this page to a colleague
The generic ingredient in FAMCICLOVIR is famciclovir. There are eight drug master file entries for this compound. Ten suppliers are listed for this compound. Additional details are available on the famciclovir profile page.
Summary for 202438
Tradename: | FAMCICLOVIR |
Applicant: | Hetero Labs Ltd V |
Ingredient: | famciclovir |
Patents: | 0 |
Pharmacology for NDA: 202438
Mechanism of Action | DNA Polymerase Inhibitors |
Suppliers and Packaging for NDA: 202438
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
FAMCICLOVIR | famciclovir | TABLET;ORAL | 202438 | ANDA | Camber Pharmaceuticals, Inc. | 31722-706 | 31722-706-01 | 100 TABLET, FILM COATED in 1 BOTTLE (31722-706-01) |
FAMCICLOVIR | famciclovir | TABLET;ORAL | 202438 | ANDA | Camber Pharmaceuticals, Inc. | 31722-706 | 31722-706-05 | 500 TABLET, FILM COATED in 1 BOTTLE (31722-706-05) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 125MG | ||||
Approval Date: | Sep 10, 2014 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 250MG | ||||
Approval Date: | Sep 10, 2014 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 500MG | ||||
Approval Date: | Sep 10, 2014 | TE: | AB | RLD: | No |
Complete Access Available with Subscription