← FDA DRUG APPROVALS

FDA NDA · NDA007513

LEVOPHED

norepinephrine bitartrate

Sponsor: HOSPIRA

APPLICATION
NDA007513
TYPE
NDA
ORIGINAL APPROVAL
1950-07-13
LATEST ACTION
2020-10-21
ROUTE
INTRAVENOUS, INJECTION
DOSAGE FORM
INJECTABLE
MARKETING STATUS
Prescription

Products

LEVOPHED · ReferencePrescription
NOREPINEPHRINE BITARTRATE EQ 1MG BASE/ML · INJECTABLE · INJECTION

Approval history

2020-10-21Labeling · Supplement 45 · standardLetterAP
2020-06-15Labeling · Supplement 38 · standardLetterAP
2007-09-26Manufacturing (CMC) · Supplement 24LetterAP
1999-09-20Labeling · Supplement 22 · standardAP
1991-09-13Labeling · Supplement 21AP
1991-06-12Manufacturing (CMC) · Supplement 20 · priorityAP
1989-04-06Labeling · Supplement 16AP
1988-03-02Labeling · Supplement 19AP
1987-05-27Labeling · Supplement 18AP
1985-01-14Labeling · Supplement 17AP
1978-04-14Manufacturing (CMC) · Supplement 15 · priorityAP
1977-02-14REMS · Supplement 9 · priorityAP
1950-07-13Type 1 - New Molecular Entity · Original · priorityAP
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 →