Cabergoline (Page 4 of 4)

OVERDOSAGE

Overdosage might be expected to produce nasal congestion, syncope, or hallucinations. Measures to support blood pressure should be taken if necessary.

DOSAGE AND ADMINISTRATION

The recommended dosage of Cabergoline Tablets, USP for initiation of therapy is 0.25 mg twice a week. Dosage may be increased by 0.25 mg twice weekly up to a dosage of 1 mg twice a week according to the patient’s serum prolactin level. Before initiating treatment, cardiovascular evaluation should be performed and echocardiography should be considered to assess for valvular disease.

Dosage increases should not occur more rapidly than every 4 weeks, so that the physician can assess the patient’s response to each dosage level. If the patient does not respond adequately, and no additional benefit is observed with higher doses, the lowest dose that achieved maximal response should be used and other therapeutic approaches considered. Patients receiving long term treatment with cabergoline should undergo periodic assessment of their cardiac status and echocardiography should be considered.

After a normal serum prolactin level has been maintained for 6 months, cabergoline may be discontinued, with periodic monitoring of the serum prolactin level to determine whether or when treatment with cabergoline should be reinstituted. The durability of efficacy beyond 24 months of therapy with cabergoline has not been established.

HOW SUPPLIED

Cabergoline Tablets, USP are white to off-white, oval shaped, flat face, beveled edge tablet containing 0.5 mg Cabergoline USP. Each tablet is scored on one side and has the letters “IN” and the letter “G” on either side of breakline. The other side of the tablet is engraved with the number “118”.

Cabergoline Tablets, USP are available as follows:

Bottle of 8 tablets NDC 50742-118-08

Storage

Store at 20° to 25°C (68° to 77°F) [see USP controlled room temperature].

Dispense in original container.

Rx only

Manufactured for:

Ingenus Pharmaceuticals, LLC

Orlando, FL 32839-6408

Made in India

Revised: 07/2019

ingenus logoingenus logo

DRUG: Cabergoline

GENERIC: Cabergoline

DOSAGE: TABLET

ADMINSTRATION: ORAL

NDC: 70518-2379-0

NDC: 70518-2379-1

COLOR: white

SHAPE: OVAL

SCORE: Two even pieces

SIZE: 2 mm

IMPRINT: IN;G;118

PACKAGING: 1 in 1 POUCH

OUTER PACKAGING: 8 in 1 BOX, UNIT-DOSE

ACTIVE INGREDIENT(S):

  • CABERGOLINE 0.5mg in 1

INACTIVE INGREDIENT(S):

  • CELLULOSE, MICROCRYSTALLINE
  • CITRIC ACID MONOHYDRATE
  • CROSCARMELLOSE SODIUM
  • MAGNESIUM STEARATE
Remedy_Label
(click image for full-size original)
MM4
(click image for full-size original)
CABERGOLINE cabergoline tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:70518-2379(NDC:50742-118)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CABERGOLINE (CABERGOLINE) CABERGOLINE 0.5 mg
Inactive Ingredients
Ingredient Name Strength
CELLULOSE, MICROCRYSTALLINE
CROSCARMELLOSE SODIUM
CITRIC ACID MONOHYDRATE
MAGNESIUM STEARATE
Product Characteristics
Color white (White) Score 2 pieces
Shape OVAL (OVAL) Size 2mm
Flavor Imprint Code IN;G;118
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70518-2379-0 8 POUCH in 1 BOX, UNIT-DOSE contains a POUCH (70518-2379-1)
1 NDC:70518-2379-1 1 TABLET in 1 POUCH This package is contained within the BOX, UNIT-DOSE (70518-2379-0)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA204735 10/23/2019
Labeler — REMEDYREPACK INC. (829572556)

Revised: 01/2021 REMEDYREPACK INC.

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