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FDA ANDA · ANDA062391

DOXYCYCLINE HYCLATE

Sponsor: MUTUAL PHARM

APPLICATION
ANDA062391
TYPE
ANDA
ORIGINAL APPROVAL
1982-09-30
LATEST ACTION
1998-12-01
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

DOXYCYCLINE HYCLATEDiscontinued
DOXYCYCLINE HYCLATE EQ 100MG BASE · TABLET · ORAL

Approval history

1998-12-01Manufacturing (CMC) · Supplement 26AP
1995-08-11Manufacturing (CMC) · Supplement 25AP
1994-12-23Manufacturing (CMC) · Supplement 24AP
1994-10-11Manufacturing (CMC) · Supplement 23AP
1993-12-13Labeling · Supplement 22AP
1993-07-22Labeling · Supplement 21AP
1992-05-01Labeling · Supplement 20AP
1992-04-03Manufacturing (CMC) · Supplement 17AP
1992-04-03Manufacturing (CMC) · Supplement 19AP
1992-01-10Labeling · Supplement 16AP
1991-07-12Manufacturing (CMC) · Supplement 15AP
1991-05-29Manufacturing (CMC) · Supplement 14AP
1982-09-30OriginalAP
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Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.

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