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ACYCLOVIR از شرکت ACTAVIS ELIZABETH

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اطلاعات داروی نمایش داده شده مستقیما از دیتابیس اطلاعات دارویی سازمان غذا و دارو آمریکا (FDA) استخراج می شود و مرتبا به روز رسانی می شود
داروی نمایش داده شده مورد تایید FDA می باشد و اطلاعات ثبت آن در زیر قابل مشاهده است

ACYCLOVIR از شرکت ACTAVIS ELIZABETH

Abbreviated New Drug Application (ANDA): 074906

Company: ACTAVIS ELIZABETH

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
ACYCLOVIR ACYCLOVIR 200MG CAPSULE;ORAL Discontinued

None

No No
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
08/26/1997 ORIG-1 Approval

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
10/28/2004 SUPPL-14 Labeling

Label is not available on this site.

04/23/2002 SUPPL-7 Labeling

Label is not available on this site.

11/02/2001 SUPPL-6 Manufacturing (CMC)-Control

Label is not available on this site.

05/01/2001 SUPPL-5 Manufacturing (CMC)-Control

Label is not available on this site.

03/08/2001 SUPPL-4 Manufacturing (CMC)-Control

Label is not available on this site.

07/17/2000 SUPPL-3 Labeling

Label is not available on this site.

08/10/1998 SUPPL-2 Labeling

Label is not available on this site.

03/26/1998 SUPPL-1 Labeling

Label is not available on this site.

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