Goniotaire

Product NDC: 59390-182
Requested package NDC: 59390-182-13
11-digit product format: 593900182
Labeler code: 59390
Product ID: 59390-182_3e98cefc-43d0-40bf-80be-651f17a39d4f
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: HYPROMELLOSE 2906 (4000 MPA.S)
Dosage form: SOLUTION
Route: OPHTHALMIC
Labeler: Altaire Pharmaceuticals Inc.
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2002-01-18
Marketing end: 0000-00-00
Substance: HYPROMELLOSE 2906 (4000 MPA.S)
Active strength: 25 mg/mL
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	59390-182	59390-182-13	D	Discontinued by firm		2026-10-05

Reported adverse events (FAERS/openFDA)#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
59390-182-13	Goniotaire	15 mL in 1 BOTTLE	SOLUTION	15		3
59390-182-13	Goniotaire	1 in 1 CARTON	SOLUTION	1		3

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
59390-182-13	ML - Milliliter	59390-182	8d317a1f-e2f5-4871-bd9b-db280399fff2	1	2018-11-06

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59390-182	GONIOTAIRE (HYPROMELLOSE 2906 (4000 MPA.S)) SOLUTION [ALTAIRE PHARMACEUTICALS INC.]	3	Legacy NDC, 2 package rows	20221101_9ebedd36-523a-4f92-8fe9-33beaf7288f9.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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Goniotaire	HYPROMELLOSE 2906 (4000 MPA.S)	Altaire Pharmaceuticals Inc.	9ebedd36-523a-4f92-8fe9-33beaf7288f9	2022-10-28	Warnings	Exact identifier ndc (package): 59390-182-13 ndc (product): 59390-182 ndc11 (package): 59390018213

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
5EYA69XGAT	HYPROMELLOSE 2906 (4000 MPA.S)	9004-65-3	HYPROMELLOSE 2906 (4000 MPA.S)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
310934	hypromellose 2.5 % Ophthalmic Solution	PSN	9ebedd36-523a-4f92-8fe9-33beaf7288f9	3
310934	hypromellose 25 MG/ML Ophthalmic Solution	SCD	9ebedd36-523a-4f92-8fe9-33beaf7288f9	3
310934	hypromellose 2.5 % Ophthalmic Solution	SY	9ebedd36-523a-4f92-8fe9-33beaf7288f9	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
59390-182-13	59390018213	1 BOTTLE in 1 CARTON (59390-182-13) > 15 mL in 1 BOTTLE	1 bottle	2002-01-18	0000-00-00	No	No	Current