Pred Phos - Gati

Manufacturer
Imprimis NJOF, LLC
Effective date
2018-06-08
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:53:51

Label at a glance#

ProductPred Phos - Gati
Active ingredientPREDNISOLONE SODIUM PHOSPHATE, GATIFLOXACIN
Label structure2 sections

Storage and handling

Store at 20° to 25° C (68° to 77° F)​

Label contents#

Full prescribing information#

STORAGE AND HANDLING SECTION


Store at 20° to 25° C (68° to 77° F)​

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle LabelBottle Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71384-551-032020-02-12C16284748780-19d75b9d0-ab82-f424-e053-dadaa90a57ce6e284a6a-7c81-bf88-e053-2991aa0a28a5
71384-551-032020-01-31C16284748780-19d75b9d0-ab82-f424-e053-dadaa90a57ce6e284a6a-7c81-bf88-e053-2991aa0a28a5

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71384-551-03ML - Milliliter71384-5510b4c7ec2-ebae-4c01-80b9-4cc1da64cb1c12018-11-06

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71384-55171384-551-03

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
PREDNISOLONE SODIUM PHOSPHATEIV021NXA9JACTIR
GATIFLOXACINL4618BD7KJACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
6e284a6a-7c82-bf88-e053-2991aa0a28a56e284a6a-7c81-bf88-e053-2991aa0a28a52018-06-08Exact identifier
spl id: 6e284a6a-7c82-bf88-e053-2991aa0a28a5
spl set id: 6e284a6a-7c81-bf88-e053-2991aa0a28a5

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.