Ondansetron
Product Images NDC 67296-0847

This is a prescription drug with the National Drug Code (NDC) number 62756-130-02. It is Ondansetron Hydrochloride Tablets, with a dosage strength of 4mg. The package contains 100 (10x10) Unit Dose Tablets. Please consult a healthcare professional before using this medication.*

This is a prescription drug with the National Drug Code (NDC) number 62756-131-02. It is Ondansetron Hydrochloride Tablets in 8mg strength, packed as 100 unit dose tablets in blister packs of 10 tablets each. This medication is available by prescription only.*

This is a description for Ondansetron Hydrochloride Tablets. Each film-coated tablet contains 5 mg of ondansetron hydrochloride, USP (dihydrate) equivalent to 4 mg of ondansetron. The usual dosage information is provided in the package insert. It is recommended to store the tablets at a temperature between 20°C to 25°C (68°F to 77°F) and protect them from light. The tablets should be dispensed in a tight, light-resistant container as per USP standards. The product is distributed by Sun Pharmaceutical Industries, Inc. and manufactured by Sun Pharmaceutical Industries Ltd. in India. The NDC number is 62756-130-01.*

This text provides information about a film-coated tablet containing 10 mg of ondansetron hydrochloride, manufactured by Sun Pharmaceutical Industries Ltd. The text also indicates typical dosage instructions and storage conditions for the medication. It is distributed by Sun Pharmaceutical Industries, Inc. in Cranbury, NJ.*

Description: This is information regarding Ondansetron Orally Disintegrating Tablets, USP. Each tablet contains 4 mg ondansetron, USP and is intended for prescription use. The tablets meet the USP Disintegration Test 2. It is advised to read the package insert for Dosage and Administration instructions. The tablets should not be removed from the blisterpack until right before use and stored at a temperature of 20° to 25°C (68° to 77°F). The product is manufactured by Sun Pharmaceutical Industries Ltd. in India and distributed by Sun Pharmaceutical Industries, Inc. in Cranbury, NJ.*

This is a description of Ondansetron Orally Disintegrating Tablets, USP. Each tablet contains 8 mg ondansetron, USP and is intended for oral use. The product is manufactured by Sun Pharmaceutical Industries Ltd. in Gujarat, India, and distributed by Sun Pharmaceutical Industries, Inc. in Cranbury, NJ. The tablets should be kept in a cool, controlled room temperature environment and should not be removed from the blister pack until immediately before use. The packaging includes 30 tablets in 3 blister cards, each containing 10 tablets. The package insert provides information about dosage, administration, and storage recommendations. It also mentions that the product meets the USP Disintegration Test 2 standard.*

This information provides details about Ondansetron Orally Disintegrating Tablets containing 4 mg of ondansetron, USP. The tablets are suitable for usage by Phenylketonurics and meet the USP Disintegration Test 2 standards. For dosage and administration instructions, refer to the package insert. Store the tablets at a temperature between 20°C to 25°C (68°F to 77°F). Manufactured by Sun Pharmaceutical Industries Ltd., the product is distributed by Sun Pharmaceutical Industries, Inc., located in Cranbury, New Jersey. The National Drug Code (NDC) for this product is 62756-240-83. The tablets are available in a pack of 30 and are prescription-only medication. The manufacturing address is Halol-Baroda Highway, Halol-389 350, Gujarat, India, with additional details such as the Global Trade Identification Number (GTIN), serial number (SN), LOT number, and expiration date provided.*

This text provides information about a medicine in the form of orally disintegrating tablets containing 8 mg ondansetron, USP. It mentions the presence of phenylalanine and advises to refer to the package insert for dosage and administration guidelines. The tablets meet USP Disintegration Test 2 and should be stored at room temperature. The product is distributed by Sun Pharmaceutical Industries, Inc. in Cranbury, NJ. Manufacturing information indicates that they are made by Sun Pharmaceutical Industries Ltd. in Gujarat, India. It also includes a National Drug Code (NDC) and a lot number.*