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Paromomycin

Generic Name: Paromomycin sulfate
Dosage Form: capsule

Paromomycin Description

Paromomycin sulfate is a broad spectrum antibiotic produced by Streptomyces riomosus var. Paromomycinus. It is a white, amorphous, stable, water-soluble product. Paromomycin sulfate is designated chemically as O-2,6-Diamino-2,6-dideoxy-β-L-idopyranosyl-(1→3)-O-β-D- ribofuranosyl-(1→5)-O-[2-amino-2-deoxy-α-D-glucopyranosyl-(1→4)]-2-deoxystreptamine sulfate (salt). The molecular formula is C23H45N5O14xH2SO4, with a molecular weight of 615.64 (base). Its structural formula is:





Each capsule, for oral administration, contains Paromomycin sulfate equivalent to 250 mg Paromomycin. Each capsule also contains the following inactive ingredients: FD&C Green #3; FD&C Yellow #5 (tartrazine); gelatin, NF; and titanium dioxide, USP.

Paromomycin - Clinical Pharmacology

The in vitro and in vivo antibacterial action of Paromomycin closely parallels that of neomycin. It is poorly absorbed after oral administration, with almost 100% of the drug recoverable in the stool.

Indications and Usage for Paromomycin

Paromomycin sulfate is indicated for intestinal amebiasis—acute and chronic (NOTE—It is not effective in extraintestinal amebiasis); management of hepatic coma—as adjunctive therapy.

Contraindications

Paromomycin sulfate is contraindicated in individuals with a history of previous hypersensitivity reactions to it. It is also contraindicated in intestinal obstruction.

Precautions

The use of this antibiotic, as with other antibiotics, may result in an overgrowth of nonsusceptible organisms, including fungi. Constant observation of the patient is essential. If new infections caused by nonsusceptible organisms appear during therapy, appropriate measures should be taken.

The drug should be used with caution in individuals with ulcerative lesions of the bowel to avoid renal toxicity through inadvertent absorption.

This product contains FD&C Yellow No. 5 (tartrazine) which may cause allergic-type reactions (including bronchial asthma) in certain susceptible persons. Although the overall incidence of FD&C Yellow No. 5 (tartrazine) sensitivity in the general population is low, it is frequently seen in patients who also have aspirin hypersensitivity.

Adverse Reactions

Nausea, abdominal cramps, and diarrhea have been reported in patients on doses over 3 g daily.

Paromomycin Dosage and Administration

Intestinal amebiasis: Adults and Children: Usual dose—25 to 35 mg/kg body weight daily, administered in three doses with meals, for five to ten days.


Management of hepatic coma: Adults: Usual dose—4 g daily in divided doses, given at regular intervals for five to six days.

How is Paromomycin Supplied

Paromomycin Sulfate Capsules, each contain Paromomycin sulfate equivalent to 250 mg Paromomycin. The capsule is green/yellow, imprinted "175" in black ink on the cap and body.


NDC 57664-175-08: Bottles of 100

Store at controlled room temperature 15° to 30°C (59° to 86°F).

Protect from moisture.

Caution—Federal law prohibits dispensing without prescription.

Manufactured by:

ALKALOIDA Chemical Company Zrt.
4440 Tiszavasvári

Kabay János u. 29.

Hungary


Distributed by:

Sun Pharmaceutical Industries, Inc.

Cranbury, NJ 08512


Revised: 04/2015

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Paromomycin Capsules, USP 250 mg
NDC 57664-175-08
Rx Only
100 Tablets
ALKALOIDA Chemical Company Zrt.


Paromomycin SULFATE 
Paromomycin sulfate capsule
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:57664-175
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Paromomycin SULFATE (Paromomycin) Paromomycin SULFATE 250 mg
Inactive Ingredients
Ingredient Name Strength
FD&C GREEN NO. 3  
FD&C YELLOW NO. 5  
GELATIN  
TITANIUM DIOXIDE  
Product Characteristics
Color GREEN, YELLOW Score no score
Shape CAPSULE Size 19mm
Flavor Imprint Code 175
Contains         
Packaging
# Item Code Package Description
1 NDC:57664-175-08 100 CAPSULE in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA064171 06/30/1997
Labeler - Sun Pharmaceutical Industries, Inc. (146974886)
Establishment
Name Address ID/FEI Operations
Sun Pharmaceutical Industries, Inc. 146974886 MANUFACTURE(57664-175), PACK(57664-175)
Revised: 02/2016
 
Sun Pharmaceutical Industries, Inc.
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