FDA.reportPublic FDA data

STRENZA PLUS

Product NDC
73614-732
Requested package NDC
73614-732-03
11-digit product format
736140732
Labeler code
73614
Product ID
73614-732_2df9064c-0528-4c21-e063-6294a90a56d8
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Moxifloxacin 0.5%, Bromfenac 0.09%, Prednisolone Acetate 1%
Dosage form
KIT
Route
OPHTHALMIC
Labeler
Brisk Pharmaceuticals
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2025-02-10
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
STRENZA PLUS
Listing expiration
2026-12-31

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
403818Internal RxNorm lookup
578018Internal RxNorm lookup
1376336Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
2df9064c-0527-4c21-e063-6294a90a56d8Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
b3fecff3-fb51-4f66-b443-a130905bb500Product name120250804
e42b5738-f3b2-36cb-547c-d658794618bcProduct name220250804
84b851da-be59-d750-14d1-e4d93cc3b4daProduct name920250630
3a7a0034-a88d-88c3-f43e-ea34c6a216deProduct name220250311
9dbc4744-f7be-4393-b71a-e1bfd8b97659Product name220250218
4ce8f27b-067c-45ad-b8f6-4b29ec66e497Product name220250115
b81a1117-443d-49e4-a709-58c3c32468afProduct name520241010
2194a6ab-15bb-de49-cced-f09e642b1b64Product name820240313
9e44d9f9-cb87-3b0f-4c71-c8438d0dc2e5Product name220240102
a0e37fa3-7f16-4fbf-bdb7-ae82cb1a553aProduct name120170309
af7d3306-1338-423f-839e-419aad9e8a86Product name120170309
ee6f8cae-1597-1a7e-3fb9-6aaeba954efeProduct name320150902
d7840f4c-f22a-4403-b5da-53ac6ac8fd90Product name120150728
ccc7bb05-654a-45d2-a0d6-09ab96ba531bProduct name220150611
8442aba0-7521-47cb-8a4e-c9896f35e8aeProduct name320150317
18d57d04-4a34-a130-5dd5-b7fc47f3b567Product name120140508
379bc253-901a-e6e1-92b7-0fc574249e07Product name120140508
48b05f5d-d2fc-45ab-76e8-3cb5bd44890dProduct name120140508
73adedd8-aba8-27d9-78d9-2e3c4a3cf954Product name120140508
9ae74339-0a3d-82e9-5dd1-88bd2607bd6bProduct name120140508
9f10552a-9a7b-8e6c-3223-dc44310af6cfProduct name120140508
e44e38a9-2d9e-b0e2-cce9-490554639f3dProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73614-732-03STRENZA PLUS1 in 1 CARTONKIT11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73614-732STRENZA PLUS (MOXIFLOXACIN 0.5%, BROMFENAC 0.09%, PREDNISOLONE ACETATE 1%) KIT [BRISK PHARMACEUTICALS]1Current NDC, 1 package rows20250215_2df9064c-0527-4c21-e063-6294a90a56d8.zip

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
STRENZA PLUSMOXIFLOXACIN 0.5%, BROMFENAC 0.09%, PREDNISOLONE ACETATE 1%Brisk Pharmaceuticals2df9064c-0527-4c21-e063-6294a90a56d82025-02-12Exact identifier
ndc (package): 73614-732-03
ndc (product): 73614-732
ndc11 (package): 73614073203

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
578018bromfenac 0.09 % Ophthalmic SolutionPSN2df9064c-0527-4c21-e063-6294a90a56d81
403818moxifloxacin HCl 0.5 % Ophthalmic SolutionPSN2df9064c-0527-4c21-e063-6294a90a56d81
1376336prednisoLONE acetate 1 % Ophthalmic SuspensionPSN2df9064c-0527-4c21-e063-6294a90a56d81
578018bromfenac 0.9 MG/ML Ophthalmic SolutionSCD2df9064c-0527-4c21-e063-6294a90a56d81
403818moxifloxacin 5 MG/ML Ophthalmic SolutionSCD2df9064c-0527-4c21-e063-6294a90a56d81
1376336prednisolone acetate 10 MG/ML Ophthalmic SuspensionSCD2df9064c-0527-4c21-e063-6294a90a56d81
578018bromfenac 0.09 % Ophthalmic SolutionSY2df9064c-0527-4c21-e063-6294a90a56d81
578018bromfenac 0.9 MG/ML (bromfenac sodium 1.035 MG/ML) Ophthalmic SolutionSY2df9064c-0527-4c21-e063-6294a90a56d81
403818moxifloxacin (as moxifloxacin HCl) 0.5 % Ophthalmic SolutionSY2df9064c-0527-4c21-e063-6294a90a56d81
1376336prednisolone acetate 1 % Ophthalmic SuspensionSY2df9064c-0527-4c21-e063-6294a90a56d81

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
73614-732-03736140732031 KIT in 1 CARTON (73614-732-03) * 5 mL in 1 BOTTLE, PLASTIC * 1 BOTTLE, DROPPER in 1 CARTON (72266-142-01) / 1.7 mL in 1 BOTTLE, DROPPER * 3 mL in 1 BOTTLE1 kit2025-02-10NoNoCurrent