FDA ANDA · ANDA074794

RANITIDINE

Sponsor: ACTAVIS ELIZABETH

APPLICATION

ANDA074794

TYPE

ANDA

ROUTE

Oral

DOSAGE FORM

Solution

MARKETING STATUS

None (Tentative Approval)

Products

RANITIDINENone (Tentative Approval)

RANITIDINE 15MG/ML · Solution · Oral

1997-11-18OriginalTA

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

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