← FDA DRUG APPROVALS

FDA NDA · NDA016677

SODIUM CHLORIDE

Sponsor: BAXTER HLTHCARE

APPLICATION
NDA016677
TYPE
NDA
ORIGINAL APPROVAL
1970-12-09
LATEST ACTION
2024-07-24
ROUTE
INTRAVENOUS, INJECTION
DOSAGE FORM
SOLUTION
MARKETING STATUS
Prescription

Products

SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER · ReferencePrescription
SODIUM CHLORIDE 450MG/50ML (9MG/ML) · SOLUTION · INJECTION
SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER · ReferencePrescription
SODIUM CHLORIDE 900MG/100ML · SOLUTION · INJECTION
SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER · ReferencePrescription
SODIUM CHLORIDE 225MG/25ML (9MG/ML) · SOLUTION · INJECTION

Approval history

2024-07-24Labeling · Supplement 185 · standardLetterAP
2019-05-29Labeling · Supplement 169 · standardLabelAP
2018-03-09Manufacturing (CMC) · Supplement 160LabelAP
2016-03-03Manufacturing (CMC) · Supplement 151 · standardLabelAP
2015-05-13Manufacturing (CMC) · Supplement 150 · standardLabelAP
2014-12-22Labeling · Supplement 148 · standardLetterAP
2014-06-05Manufacturing (CMC) · Supplement 149 · standardAP
2013-09-11Labeling · Supplement 147 · standardLetterAP
2005-08-26Supplement · Supplement 139 · standardLetterAP
2005-05-23Labeling · Supplement 137 · standardLetterAP
2003-07-17Manufacturing (CMC) · Supplement 131 · standardLetterAP
2002-09-16Manufacturing (CMC) · Supplement 128 · standardAP
2002-04-03Labeling · Supplement 124 · standardLetterAP
2001-08-14Manufacturing (CMC) · Supplement 126 · standardAP
1999-11-24Manufacturing (CMC) · Supplement 125 · standardAP
1997-12-31Manufacturing (CMC) · Supplement 123 · standardAP
1997-06-10Manufacturing (CMC) · Supplement 121 · standardAP
1997-04-29Manufacturing (CMC) · Supplement 122 · standardAP
1996-11-14Manufacturing (CMC) · Supplement 119 · standardAP
1996-10-11Manufacturing (CMC) · Supplement 120 · standardAP
1995-09-27Manufacturing (CMC) · Supplement 118 · standardAP
1994-09-30Manufacturing (CMC) · Supplement 116 · standardAP
1994-02-18Manufacturing (CMC) · Supplement 117 · standardAP
1993-06-01Manufacturing (CMC) · Supplement 111 · standardAP
1993-01-06Manufacturing (CMC) · Supplement 115 · standardAP
1992-11-23Manufacturing (CMC) · Supplement 110 · standardAP
1991-03-26Manufacturing (CMC) · Supplement 109 · standardAP
1991-02-15Manufacturing (CMC) · Supplement 106 · standardAP
1990-05-24Manufacturing (CMC) · Supplement 108 · standardAP
1990-03-23Manufacturing (CMC) · Supplement 107 · standardAP
1989-07-26Manufacturing (CMC) · Supplement 105 · standardAP
1989-01-12Manufacturing (CMC) · Supplement 104 · standardAP
1989-01-10Manufacturing (CMC) · Supplement 102 · standardAP
1988-06-14Manufacturing (CMC) · Supplement 103 · standardAP
1987-07-25Manufacturing (CMC) · Supplement 100 · standardAP
1987-05-28Manufacturing (CMC) · Supplement 99 · standardAP
1987-04-27Manufacturing (CMC) · Supplement 101 · standardAP
1986-02-27Manufacturing (CMC) · Supplement 96 · standardAP
1985-10-30Labeling · Supplement 89AP
1985-10-30Manufacturing (CMC) · Supplement 88 · standardAP
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 →