Nystatin NYSTATIN PAI HOLDINGS, LLC DBA PAI PHARMA FDA Approved Nystatin is an antimycotic polyene antibiotic obtained from Streptomyces noursei . Structural formula: C 47 H 75 NO 17 MW 926.13 Nystatin Oral Suspension USP, for oral administration, contains 100,000 USP Nystatin Units per mL. Inactive ingredients: alcohol (≤ 1% v/v), cherry flavor, citric acid, D&C Yellow No. 10, FD&C Red No. 40, glycerin, magnesium aluminum silicate, methylparaben, potassium phosphate dibasic, propylene glycol, propylparaben, purified water and sucrose. Chemical structure
FunFoxMeds bottle
Substance Nystatin
Route
ORAL
Applications
ANDA203621
Package NDC

Drug Facts

Composition & Profile

Strengths
60 ml 473 ml 5 ml 40 unit 10 unit 50 unit 100 unit
Quantities
60 ml 473 ml 5 ml
Treats Conditions
Indications And Usage Nystatin Oral Suspension Is Indicated For The Treatment Of Candidiasis In The Oral Cavity
Pill Appearance
Color: yellow

Identifiers & Packaging

Container Type BOTTLE
All Product Codes
UNII
BDF1O1C72E
Packaging

HOW SUPPLIED Nystatin Oral Suspension USP, 100,000 USP Nystatin Units per mL, is available in a cherry flavored, light creamy yellow, ready-to-use suspension, supplied in the following oral dosage forms: NDC 0121-1045-02: 2 fl oz (60 mL) bottle with calibrated dropper NDC 0121-1045-16: 16 fl oz (473 mL) bottle NDC 0121-4045-05: 5 mL unit dose cup. Case contains 40 unit dose cups of 5 mL (NDC 0121-4045-40) packaged in 4 trays of 10 unit dose cups each, 50 unit dose cups of 5 mL (NDC 0121-4045-50) packaged in 5 trays of 10 unit dose cups each and 100 unit dose cups of 5 mL (NDC 0121-4045-00) packaged in 10 trays of 10 unit dose cups each. Storage Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. Avoid freezing.; PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label NDC 0121-1045-16 Nystatin Oral Suspension, USP 100,000 units per mL SHAKE WELL BEFORE USING Cherry Flavored Rx only 16 fl oz (473 mL) PAI Pharma Greenville, SC 29605 Nystatin-473 mL

Package Descriptions
  • HOW SUPPLIED Nystatin Oral Suspension USP, 100,000 USP Nystatin Units per mL, is available in a cherry flavored, light creamy yellow, ready-to-use suspension, supplied in the following oral dosage forms: NDC 0121-1045-02: 2 fl oz (60 mL) bottle with calibrated dropper NDC 0121-1045-16: 16 fl oz (473 mL) bottle NDC 0121-4045-05: 5 mL unit dose cup. Case contains 40 unit dose cups of 5 mL (NDC 0121-4045-40) packaged in 4 trays of 10 unit dose cups each, 50 unit dose cups of 5 mL (NDC 0121-4045-50) packaged in 5 trays of 10 unit dose cups each and 100 unit dose cups of 5 mL (NDC 0121-4045-00) packaged in 10 trays of 10 unit dose cups each. Storage Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. Avoid freezing.
  • PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label NDC 0121-1045-16 Nystatin Oral Suspension, USP 100,000 units per mL SHAKE WELL BEFORE USING Cherry Flavored Rx only 16 fl oz (473 mL) PAI Pharma Greenville, SC 29605 Nystatin-473 mL

Overview

Nystatin is an antimycotic polyene antibiotic obtained from Streptomyces noursei . Structural formula: C 47 H 75 NO 17 MW 926.13 Nystatin Oral Suspension USP, for oral administration, contains 100,000 USP Nystatin Units per mL. Inactive ingredients: alcohol (≤ 1% v/v), cherry flavor, citric acid, D&C Yellow No. 10, FD&C Red No. 40, glycerin, magnesium aluminum silicate, methylparaben, potassium phosphate dibasic, propylene glycol, propylparaben, purified water and sucrose. Chemical structure

Indications & Usage

Nystatin Oral Suspension is indicated for the treatment of candidiasis in the oral cavity.

Dosage & Administration

INFANTS: 2 mL (200,000 units) four times daily (in infants and young children, use dropper to place one-half of dose in each side of mouth and avoid feeding for 5 to 10 minutes). NOTE: Limited clinical studies in premature and low birth weight infants indicate that 1 mL four times daily is effective. CHILDREN AND ADULTS: 4 to 6 mL (400,000 to 600,000 units) four times daily (one-half of dose in each side of mouth). The preparation should be retained in the mouth as long as possible before swallowing. Continue treatment for at least 48 hours after perioral symptoms have disappeared and cultures demonstrate eradication of Candida albicans .

Warnings & Precautions
No warnings available yet.
Contraindications

The preparation is contraindicated in patients with a history of hypersensitivity to any of its components.

Adverse Reactions

Nystatin is well tolerated even with prolonged therapy. Oral irritation and sensitization have been reported. (See PRECAUTIONS: General ). Gastrointestinal: Diarrhea (including one case of bloody diarrhea), nausea, vomiting, gastrointestinal upset/disturbances. Dermatologic: Rash, including urticaria has been reported rarely. Stevens-Johnson syndrome has been reported very rarely. Other: Tachycardia, bronchospasm, facial swelling, and non-specific myalgia have also been rarely reported. To report SUSPECTED ADVERSE REACTIONS, contact PAI Pharma at 1-800-845-8210 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

Storage & Handling

Storage Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. Avoid freezing.


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