← FDA DRUG APPROVALS

FDA ANDA · ANDA070576

MUCOSIL-20

Sponsor: DEY

APPLICATION
ANDA070576
TYPE
ANDA
ORIGINAL APPROVAL
1986-10-14
LATEST ACTION
2001-06-14
ROUTE
INHALATION, ORAL
DOSAGE FORM
SOLUTION
MARKETING STATUS
Discontinued

Products

MUCOSIL-20Discontinued
ACETYLCYSTEINE 20% · SOLUTION · INHALATION, ORAL

Approval history

2001-06-14Manufacturing (CMC) · Supplement 28AP
2000-03-21Manufacturing (CMC) · Supplement 30AP
2000-03-21Manufacturing (CMC) · Supplement 29AP
1999-06-25Labeling · Supplement 27AP
1998-11-25Labeling · Supplement 24AP
1998-02-20Labeling · Supplement 23AP
1997-09-05Manufacturing (CMC) · Supplement 22AP
1996-04-24Manufacturing (CMC) · Supplement 21AP
1994-03-11Manufacturing (CMC) · Supplement 20AP
1992-06-29Labeling · Supplement 19AP
1990-10-26Labeling · Supplement 17AP
1990-07-19Labeling · Supplement 16AP
1989-08-01Labeling · Supplement 13AP
1989-08-01Manufacturing (CMC) · Supplement 14AP
1989-08-01Manufacturing (CMC) · Supplement 15AP
1989-04-20Manufacturing (CMC) · Supplement 11AP
1988-09-29Labeling · Supplement 10AP
1988-04-20Labeling · Supplement 6AP
1987-06-16Manufacturing (CMC) · Supplement 1AP
1987-06-16Labeling · Supplement 4AP
1987-06-16Manufacturing (CMC) · Supplement 2AP
1987-06-16Manufacturing (CMC) · Supplement 3AP
1987-01-22Manufacturing (CMC) · Supplement 5AP
1986-10-14OriginalAP
VIEW ON DRUGS@FDA ↗

Related on SPEQ

Pharma industryGMP disciplineFDA drug shortagesFDA enforcement & recalls

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.

Weekly Briefing

Get the Weekly GxP Briefing

Curated regulatory intelligence — enforcement, recalls, guidance, and quality signals — in one practitioner-grade email each week. Free.

Read a past issue →