Dorzolamide PF

Manufacturer: ImprimisRx NJ
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#

ProductDorzolamide PF

Active ingredientDORZOLAMIDE HYDROCHLORIDE

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)

Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
310015	dorzolamide HCl 2 % Ophthalmic Solution	PSN	1
310015	dorzolamide 20 MG/ML Ophthalmic Solution	SCD	1
310015	dorzolamide 2 % Ophthalmic Solution	SY	1
310015	dorzolamide 20 MG/ML (as dorzolamide HCl 22.3 MG/ML) Ophthalmic Solution	SY	1

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
DORZOLAMIDE Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
973dd458-49b1-1bb1-62c6-b37c4b15fe1f	Product name	5	20251121
03f77cb2-b4ad-3c11-8781-787b5ece4291	Product name	3	20240507
97dad5a2-c524-a7b5-dede-82edefe9ce62	Product name	7	20220929

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
70261-516-10	2020-01-31	C162847	48780-1	9d75b9d0-aa68-f424-e053-dadaa90a57ce	6bb681e9-0fc7-7e5c-e053-2991aa0a7c65

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70261-516-10	Dorzolamide PF	10 mL in 1 BOTTLE, DROPPER	SOLUTION/ DROPS	10		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70261-516	DORZOLAMIDE PF SOLUTION/ DROPS [IMPRIMISRX NJ]	1	Legacy NDC, 1 package rows	20180508_6bb681e9-0fc7-7e5c-e053-2991aa0a7c65.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

Dorzolamide PF
DORZOLAMIDE HYDROCHLORIDE
DORZOLAMIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
70261-516	70261-516-10

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
Name	UNII	Kind
DORZOLAMIDE HYDROCHLORIDE	QZO5366EW7	ACTIM

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
6bb681e9-0fc8-7e5c-e053-2991aa0a7c65			6bb681e9-0fc7-7e5c-e053-2991aa0a7c65	2018-05-08		Exact identifier spl id: 6bb681e9-0fc8-7e5c-e053-2991aa0a7c65 spl set id: 6bb681e9-0fc7-7e5c-e053-2991aa0a7c65

Reported adverse events (FAERS/openFDA)#

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