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BRETYLIUM TOSYLATE از شرکت HOSPIRA

تصویر پیدا نشد !

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

BRETYLIUM TOSYLATE از شرکت HOSPIRA

New Drug Application (NDA): 019033

Company: HOSPIRA

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
BRETYLIUM TOSYLATE BRETYLIUM TOSYLATE 50MG/ML INJECTABLE;INJECTION 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
04/16/1986 ORIG-1 Approval

Type 5 – New Formulation or New Manufacturer

STANDARD

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
06/28/2001 SUPPL-8 Manufacturing (CMC)-Expiration Date

Label is not available on this site.

10/15/1998 SUPPL-7 Manufacturing (CMC)-Control

Label is not available on this site.

08/26/1999 SUPPL-6 Labeling

Label is not available on this site.

08/07/1996 SUPPL-5 Manufacturing (CMC)-Control

Label is not available on this site.

03/04/1994 SUPPL-3 Labeling

Label is not available on this site.

08/20/1990 SUPPL-2 Manufacturing (CMC)-Expiration Date

Label is not available on this site.

11/22/1988 SUPPL-1 Manufacturing (CMC)-Control

Label is not available on this site.

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