CLEMASTINE FUMARATE از شرکت ACTAVIS MID ATLANTIC

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

CLEMASTINE FUMARATE از شرکت ACTAVIS MID ATLANTIC

Abbreviated New Drug Application (ANDA): 074075

Company: ACTAVIS MID ATLANTIC

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
CLEMASTINE FUMARATE CLEMASTINE FUMARATE EQ 0.5MG BASE/5ML SYRUP;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
10/31/1993 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
12/04/2000 SUPPL-8 Manufacturing (CMC)-Expiration Date

Label is not available on this site.

12/04/2000 SUPPL-7 Manufacturing (CMC)-Control

Label is not available on this site.

03/27/2000 SUPPL-6 Manufacturing (CMC)-Expiration Date

Label is not available on this site.

03/27/2000 SUPPL-5 Labeling

Label is not available on this site.

03/27/2000 SUPPL-4 Manufacturing (CMC)-Packaging

Label is not available on this site.

02/08/1994 SUPPL-1 Labeling

Label is not available on this site.

بخوانید  CLEMASTINE FUMARATE از شرکت ANI PHARMS
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