loader
Please Wait
Applying Filters...

Athena Athena

X

Looking for Controlled & Modified Release? Find Controlled & Modified Release Agents used in Selenium Sulfide to address drug delivery challenges on PharmaCompass.

Filters Filter
Cross PopUp
FILTER :

filter

01 Evonik (2)

02 Gangwal Healthcare (2)

03 Actylis (4)

04 BASF (5)

05 Ideal Cures Pvt Ltd (3)

06 Kerry (14)

07 Kima Chemical (1)

08 Lonza Capsugel (1)

09 Lubrizol Life Science Health (4)

10 The Dow Chemical Company (2)

filter

01 Capsule (9)

02 Cream / Lotion / Ointment (1)

03 Emulsion (1)

04 Gel (1)

05 Granule / Pellet (1)

06 Softgel Capsule (1)

07 Tablet (23)

08 Topical Film (1)

filter

01 China (1)

02 Germany (7)

03 India (5)

04 U.S.A (25)

Close
4

Applications:

Sustained Release Tablet Matrix

Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Capsule, Tablet

Category: Coating Systems & Additives, Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: USP, EP, and JP

Technical Specifications: Not Available

ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content

Applications:

Instamodel Blend is used to provide Extended Release from the dosage form.

Ingredient(s): HPMC 2910

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Not Available

Technical Specifications: Not Available

ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content

Applications:

Immediate Release

Ingredient(s): Hydroxypropyl Methylcellulose, Starch

Dosage Form: Tablet

Category: Coating Systems & Additives, Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Customized per requirements

Technical Specifications: Not Available

ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content

Applications:

Immediate Release

Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Tablet

Category: Coating Systems & Additives, Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Customized per requirements

Technical Specifications: Not Available

ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content

Applications:

Immediate Release

Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Tablet

Category: Coating Systems & Additives, Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Customized per requirements

Technical Specifications: Not Available

ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content

Applications:

Immediate Release

Ingredient(s): Hydroxypropyl Methylcellulose, Lactose

Dosage Form: Tablet

Category: Coating Systems & Additives, Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Customized per requirements

Technical Specifications: Not Available

ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content

Applications:

Immediate Release

Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Tablet

Category: Coating Systems & Additives, Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Customized per requirements

Technical Specifications: Not Available

ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content

Applications:

It offers an enteric-release profile to the upper gastro-intestinal tract that meets the disintegration requirements for delayed-release capsules for the European, US and Japanese Phamacopoeia.

Ingredient(s): HPMC AS, Hydroxypropyl Methyl Cellulose

Dosage Form: Capsule

Category: Controlled & Modified Release, Vegetarian Capsules

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Complies with relevant European, Japanese and US Pharmacopeia monographs

Technical Specifications: Water content – less than 6%; Size #0

ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content

Applications:

Immediate Release

Ingredient(s): Glycerol, Unmodified, Hydroxypropyl Methylcellulose

Dosage Form: Tablet

Category: Coating Systems & Additives, Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Customized per requirements

Technical Specifications: Not Available

ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content

Applications:

Immediate Release

Ingredient(s): Hydroxypropyl Methylcellulose, Polydextrose Sugar

Dosage Form: Tablet

Category: Coating Systems & Additives, Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Customized per requirements

Technical Specifications: Not Available

ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content

Applications:

Carbopol® 974P NF polymer is used in oral and mucosal contact applications such as oral liquids, bioadhesive formulations, & extended release tablets. Additionally, it can be used to formulate viscous gels, emulsions & suspensions.

Ingredient(s): Carbomer Homopolymer Type B

Dosage Form: Cream / Lotion / Ointment, Emulsion, Gel, Tablet

Category: Controlled & Modified Release, Topical

Route of Administration (Grade): Oral & Topical
Pharmacopoeia Reference: United States Pharmacopeia/National Formulary (USP/NF) monograph for Carbomer Homopolymer Type B, European Pharmacopeia (Ph. Eur.), India Pharmacopeia (IP), China Pharmacopeia (ChP) mongographs for Carbomers.

Technical Specifications: Viscosity, cP (0.5 wt% at pH 7.5)- 29,400 - 39,400

ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content

Applications:

Enteric Coatings

Ingredient(s): EthylCellulose, Hydroxypropyl Methylcellulose

Dosage Form: Tablet

Category: Coating Systems & Additives, Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Customized per requirements

Technical Specifications: Not Available

ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content

SODIUM CITRATE DIHYDRATE MULTI-COMPENDIAL

URL Supplier Web Content
LM Application #LearnMore

Applications:

A & C's Sodium Citrate Dihydrate multi-compendial is a trisodium salt of citric acid.

Ingredient(s): Sodium Citrate Dihydrate Excipient

Dosage Form: Capsule, Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Multi-compendial

Technical Specifications: Not Available

ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content

SODIUM CITRATE DIHYDRATE USP-NF

URL Supplier Web Content
LM Application #LearnMore

Applications:

A & C's Sodium Citrate Dihydrate USP-NF is a trisodium salt of citric acid.

Ingredient(s): Sodium Citrate Dihydrate Excipient

Dosage Form: Capsule, Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP/NF

Technical Specifications: Not Available

ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content

Applications:

Immediate Release

Ingredient(s): Hydroxypropyl Cellulose, Hydroxypropyl Methylcellulose

Dosage Form: Tablet

Category: Coating Systems & Additives, Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Customized per requirements

Technical Specifications: Not Available

ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content

Applications:

Immediate Release

Ingredient(s): Hydroxypropyl Methylcellulose, Polyvinyl Alcohol

Dosage Form: Tablet

Category: Coating Systems & Additives, Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Customized per requirements

Technical Specifications: Not Available

ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content

Applications:

pH-independent sustained release coating for small particles, pellets, granules and tablets. Sprayable polymeric film former. Flexible. Wash resistant.

Ingredient(s): Polyvinyl Acetate, Sodium Lauryl Sulfate

Dosage Form: Capsule, Granule / Pellet, Softgel Capsule, Tablet, Topical Film

Category: Coating Systems & Additives, Controlled & Modified Release, Taste Masking

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur.: Poly(vinyl acetate) dispersion 30 per cent; USP: Polyvinyl Acetate Dispersion

Technical Specifications: Not Available

ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content
Post Enquiry
POST ENQUIRY