Drugs@FDA: FDA Approved Drug Products

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Abbreviated New Drug Application (ANDA): 060736
Company: SUN PHARM INDUSTRIES
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
TETRACYCLINE HYDROCHLORIDE TETRACYCLINE HYDROCHLORIDE 250MG CAPSULE;ORAL Discontinued None No No
TETRACYCLINE HYDROCHLORIDE TETRACYCLINE HYDROCHLORIDE 500MG 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
02/07/1980 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
07/24/2002 SUPPL-23 Manufacturing (CMC)-Control

Label is not available on this site.

02/08/2002 SUPPL-22 Manufacturing (CMC)-Facility

Label is not available on this site.

09/24/2001 SUPPL-21 Manufacturing (CMC)-Facility

Label is not available on this site.

11/02/2001 SUPPL-20 Manufacturing (CMC)-Facility

Label is not available on this site.

12/18/2000 SUPPL-19 Manufacturing (CMC)-Facility

Label is not available on this site.

12/18/2000 SUPPL-18 Manufacturing (CMC)-Facility

Label is not available on this site.

12/18/2000 SUPPL-17 Manufacturing (CMC)-Facility

Label is not available on this site.

12/18/2000 SUPPL-16 Manufacturing (CMC)-Facility

Label is not available on this site.

05/01/1992 SUPPL-15 Labeling

Label is not available on this site.

01/22/1992 SUPPL-14 Labeling

Label is not available on this site.

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