Pharmaceuticals

PEARLITOL® FLASH – MANNITOL STARCH, CO-PROCESSED

Key attributes: Optimized for the direct compression of fast oral disintegration tablets with pleasant taste and texture.

Co-processed mannitol starch

PEARLITOL® PF – MANNITOL, PYROGEN-FREE

PEARLITOL PF pyrogen-free mannitol is used for parenteral preparations and Rx injectables. As an excipient, it is an isotonic agent and a bulking agent for freeze-dried powder for injection or infusion. White or almost white crystalline powder with a maximum water content of 0.5 percent EP/USP-NF/JP compliance. Application: Excipient

AQOAT®

Shin-Etsu AQOAT (hypromellose acetate succinate) is our second enteric coating material and it was developed for aqueous coating. Shin-Etsu AQOAT was approved as a pharmaceutical excipient in Japan in 1987, and then in the United States and several European countries in 2001. In an aqueous system, a suspension containing Shin-Etsu AQOAT (fine powder), triethyl citrate as a plasticizer, talc as an anti-tacking agent, and sodium lauryl sulfate as a wetting agent is typically used. Shin-Etsu AQOAT also shows excellent performance when it is used as a carrier for solid dispersions in order to enhance solubility of poorly soluble drugs.

Betaine Anhydrous, USP/NF,EP

White crystalline powder or white crystals

CLEARGUM® CO 03

White to off-white powder, cold water swelling modified starch, waxy maize basis. Application: Excipient

Cholesterol NF

Cholesterol NF

DL - Aspartic Acid. USP/NF, EP, JP, BP

White or almost white crystalline powder or colorless crystals

DL-Serine USP/NF,EP, JP,BP

White or almost white crystalline powder or colourless crystals

Dextrose Anhydrous C

White or almost white, crystalline powder. Purified and crystallize D-glucose, without water of crystallization Application: Excipient

Dextrose Anhydrous CF

White crystalline powder. Purified and crystallize D-glucose, without water of crystallization. Application: Excipient