Latanoprost PF

Manufacturer
ImprimisRx NJ | Imprimis Pharmaceuticals
Effective date
2018-05-08
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 20:25:42

Label at a glance#

ProductLatanoprost PF
Active ingredientLATANOPROST
Label structure2 sections

Storage and handling

Store under refrigeration 2° to 8° C (36° to 46° F)

Label contents#

Full prescribing information#

STORAGE AND HANDLING SECTION

Store under refrigeration 2° to 8° C (36° to 46° F)

Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle LabelBottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
314072latanoprost 0.005 % Ophthalmic SolutionPSN1
314072latanoprost 0.05 MG/ML Ophthalmic SolutionSCD1
314072latanoprost 0.005 % Ophthalmic SolutionSY1
314072latanoprost 125 MCG per 2.5 ML Ophthalmic SolutionSY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
LATANOPROST Pharmacologic Class Indexing5Indexing - Pharmacologic Class20191108

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f6b0b05b-3bf2-088a-8ccc-e1cf01a91e86Product name420250729
de829a7d-0b51-4e4d-a051-6a6568f15688Product name120230919
203382e3-d801-4f70-866f-ebe316583560Product name120190624
e516be5e-351f-4b2e-a26b-fdff13181605Product name120181220

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70261-515-072020-01-31C16284748780-19d75b9d0-24b8-f424-e053-dadaa90a57ce6bb6aa59-65ca-2852-e053-2991aa0a087c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70261-515-07Latanoprost PF7.5 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS7.51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70261-515LATANOPROST PF SOLUTION/ DROPS [IMPRIMISRX NJ]1Legacy NDC, 1 package rows20180508_6bb6aa59-65ca-2852-e053-2991aa0a087c.zip

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70261-51570261-515-07

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
LATANOPROST6Z5B6HVF6OACTIB

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
6bb6aa59-65cb-2852-e053-2991aa0a087c6bb6aa59-65ca-2852-e053-2991aa0a087c2018-05-08Exact identifier
spl id: 6bb6aa59-65cb-2852-e053-2991aa0a087c
spl set id: 6bb6aa59-65ca-2852-e053-2991aa0a087c

Reported adverse events (FAERS/openFDA)#

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