FDA ANDA · ANDA084514

DILOR

Sponsor: SAVAGE LABS

APPLICATION

ANDA084514

TYPE

ANDA

ORIGINAL APPROVAL

1976-08-16

LATEST ACTION

1996-02-22

ROUTE

ORAL

DOSAGE FORM

TABLET

MARKETING STATUS

Discontinued

Products

DILORDiscontinued

DYPHYLLINE 200MG · TABLET · ORAL

1996-02-22Manufacturing (CMC) · Supplement 27AP

1993-03-04Manufacturing (CMC) · Supplement 26AP

1992-02-10Manufacturing (CMC) · Supplement 24AP

1992-02-10Manufacturing (CMC) · Supplement 25AP

1992-02-10Manufacturing (CMC) · Supplement 23AP

1988-11-25Manufacturing (CMC) · Supplement 21AP

1988-11-25Manufacturing (CMC) · Supplement 22AP

1983-01-13Manufacturing (CMC) · Supplement 18AP

1983-01-13Manufacturing (CMC) · Supplement 19AP

1981-11-03Manufacturing (CMC) · Supplement 3AP

1976-08-16OriginalAP

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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