APPLICATION
ANDA085003
TYPE
ANDA
ORIGINAL APPROVAL
1976-05-28
LATEST ACTION
2002-07-03
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued
Products
AMINOPHYLLINEDiscontinued
AMINOPHYLLINE 200MG · TABLET · ORAL
Approval history
2002-07-03Manufacturing (CMC) · Supplement 42AP
2000-12-11Manufacturing (CMC) · Supplement 41AP
2000-12-11Manufacturing (CMC) · Supplement 40AP
2000-01-13Manufacturing (CMC) · Supplement 39AP
1998-10-01Manufacturing (CMC) · Supplement 38AP
1996-09-24Labeling · Supplement 37AP
1995-05-26Manufacturing (CMC) · Supplement 36AP
1994-06-16Manufacturing (CMC) · Supplement 35AP
1991-11-22Labeling · Supplement 32AP
1991-11-22Manufacturing (CMC) · Supplement 30AP
1991-11-22Manufacturing (CMC) · Supplement 29AP
1991-04-02Manufacturing (CMC) · Supplement 33AP
1991-04-02Manufacturing (CMC) · Supplement 31AP
1990-10-31Labeling · Supplement 34AP
1989-01-27Manufacturing (CMC) · Supplement 27AP
1989-01-27Manufacturing (CMC) · Supplement 25AP
1989-01-27Labeling · Supplement 26AP
1988-07-20Manufacturing (CMC) · Supplement 24AP
1986-07-16Manufacturing (CMC) · Supplement 20AP
1986-07-16Manufacturing (CMC) · Supplement 19AP
1986-07-16Manufacturing (CMC) · Supplement 21AP
1985-03-11Manufacturing (CMC) · Supplement 18AP
1984-03-29Manufacturing (CMC) · Supplement 17AP
1984-02-17Manufacturing (CMC) · Supplement 15AP
1983-08-10Manufacturing (CMC) · Supplement 14AP
1982-12-01Manufacturing (CMC) · Supplement 12AP
1976-05-28OriginalAP
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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