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GONAK™Hypromellose Ophthalmic Demulcent Solution2.5% | Gonak Hypromellose [Akorn, Inc.] | BioPortfolio

13:11 EST 27th January 2019 | BioPortfolio

Note: While we endeavour to keep our records up-to-date one should not rely on these details being accurate without first consulting a professional. Click here to read our full medical disclaimer.

FOR OPHTHALMIC USE ONLY

Indications: For Professional use in gonioscopic examinations.

Directions: Fill gonioscopic prism with solution as necessary.

Storage: Store at 15° to 30°C (59° to 86°F).

To Avoid contamination, do not touch tip of container to any surface.Replace cap after using.Not for use in conjunction with hot laser treatment. If solution changes color or becomes cloudy, do not use.

DO NOT USE IF IMPRINTED SEAL ON BOTTLE NECK IS BROKEN OR MISSING

Each mL contains: Active: Hypromellose 52906, 25mg (2.5%).

Inactives: Boric Acid, Edetate Disodium, Potassium Chloride, Sodium Borate, Purified Water, Hydrochloric Acid and/or Sodium Hydroxide may be added to adjust pH (6.0 to 7.8).

Preservative: Benzalkonium Chloride 0.01%.

KEEP OUT OF REACH OF CHILDREN

Principal Display Panel Text for Container Label:

NDC 17478-064-12

Gonak™

Hypromellose

Ophthalmic

Demulcent

Solution

2.5%

For Professional Use In

Gonioscopic Examinations

FOR OPTHALMIC USE ONLY

15 mL Sterile

Principal Display Panel Text for Carton Label:

NDC 17478-064-12

Gonak™

Hypromellose

Ophthalmic

Demulcent

Solution

2.5%

For Professional Use In

Gonioscopic Examinations

15 mL

Sterile

[Akorn Logo]

Manufacturer

Akorn, Inc.

Active Ingredients

Source

Clinical Trials [3 Associated Clinical Trials listed on BioPortfolio]

Efficacy, Tolerability and Comfort of 0.3% Hypromellose Eyedrops in Patients Undergoing LASIK Surgery

This study is designed to assess the tolerability and comfort of peri-operative 0.3% hypromellose eye drops in LASIK surgery and to assess whether preoperative 0.3% hypromellose eye drops ...

Assess the Safety and Efficacy of CsA Ophthalmic Gel in Subjects With Dry Eye

The purpose of this study is to explore the efficacy and safety of CsA ophthalmic gel in the treatment of moderate to severe tear deficiency dry eye with different dosage, frequency and co...

Eyelash Growth From Application of Bimatoprost in Gel Suspension to the Base of the Eyelashes

Objective: To determine if Lumigan (bimatoprost) causes increased lash length when used in gel suspension applied to the base of the eyelashes. Methods: Subjects recruited from the Basc...

PubMed Articles [7 Associated PubMed Articles listed on BioPortfolio]

Mechanistic Elucidation of Formation of Drug-Rich Amorphous Nanodroplets by Dissolution of the Solid Dispersion Formulation.

Drug-rich amorphous nanodroplets have great potential to improve intestinal absorption of poorly water-soluble drugs. Spray-dried samples (SPDs) of glibenclamide (GLB) with hypromellose (HPMC) or hypr...

Effect of HPMCAS on recrystallization inhibition of nimodipine solid dispersions prepared by hot-melt extrusion and dissolution enhancement of nimodipine tablets.

In current study, a novel nimodipine solid dispersion (NM-SD) was prepared by hot-melt extrusion (HME) with Hypromellose methylcellulose acetate succinate (H type and fine grades, HPMCAS-HF) for its e...

Rheological and mucoadhesive properties of polysaccharide from Bletilla striata with potential use in pharmaceutics as bio-adhesive excipient.

This study described the rheological and mucoadhesive properties of one natural water-soluble polysaccharide from Bletilla striata (BSP). The rheological characteristics of BSP in aqueous solutions an...

Impact of capsule type on aerodynamic performance of inhalation products: a case study using a formoterol-lactose binary or ternary blend.

The aerodynamic performance of a dry powder for inhalation depends on the formulation and the dry powder inhaler (DPI). In the case of capsule-based DPIs, the capsule also plays a role in the powder a...

Novel hydrophilic matrix system with non-uniform drug distribution for zero-order release kinetics.

A decrease in the release rate over time is typically encountered when dealing with hydrophilic matrix systems for oral prolonged release due to progressive increase of the distance the drug molecules...

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