CARBASTAT- carbachol injection, solution 
Novartis Ophthalmics






CARBASTAT® (Carbachol Intraocular Solution, USP) 0.01% is a sterile balanced salt solution of carbachol for intraocular injection. The active ingredient is represented by the structural formula:

Image from Drug Label Content

Established name: Carbachol

Chemical name: Ethanaminium, 2-[(aminocarbonyl)oxy]-N,N,N -trimethyl-, chloride.

Each mL contains: Active: Carbachol 0.01%.

Inactive: Sodium chloride 0.64%, potassium chloride 0.075%, calcium chloride dihydrate 0.048%, magnesium chloride hexahydrate 0.03%, sodium acetate trihydrate 0.39%, sodium citrate dihydrate 0.17%, sodium hydroxide and/or hydrochloric acid to adjust pH (5.0-7.5) and water for injection USP.


Carbachol is a potent cholinergic (parasympathomimetic) agent which produces constriction of the iris and ciliary body resulting in reduction in intraocular pressure. The exact mechanism by which carbachol lowers intraocular pressure is not precisely known.


Intraocular use for obtaining miosis during surgery. In addition, Carbastat® (Carbachol Intraocular Solution USP) reduces the intensity of intraocular pressure elevation in the first 24 hours after cataract surgery.


Should not be used in those persons showing hypersensitivity to any of the components of this preparation.


For single-dose intraocular use only. Discard unused portion. Intraocular carbachol 0.01% should be used with caution in patients with acute cardiac failure, bronchial asthma, peptic ulcer, hyperthyroidism, G.I. spasm, urinary tract obstruction and Parkinson's disease.



Studies in animals to evaluate the carcinogenic potential have not been conducted.

Pregnancy: Category C. 

There are no adequate and well controlled studies in pregnant women. Carbastat® should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.

Nursing Mothers

It is not known if this medication is excreted in breast milk. Exercise caution when administering to a nursing woman.

Pediatric Use

Safety and efficacy in pediatric patients have not been established.



Corneal clouding, persistent bullous keratopathy, retinal detachment and postoperative iritis following cataract extraction have been reported.


Side effects such as flushing, sweating, epigastric distress, abdominal cramps, tightness in urinary bladder, and headache have been reported with topical or systemic application of carbachol.


Aseptically remove the sterile vial from the blister package by peeling the backing paper and dropping the vial onto a sterile tray. Withdraw the contents into a dry sterile syringe, and replace the needle with an atraumatic cannula prior to intraocular irrigation. No more than one-half milliliter should be gently instilled into the anterior chamber for the production of satisfactory miosis. It may be instilled before or after securing sutures. Miosis is usually maximal within two to five minutes after application.


CARBASTAT (Carbachol Intraocular Solution, USP) 0.01%

1.5 mL sterile glass vials in cartons of 12 (12 x 1.5 mL)

NDC 58768-735-12

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

Rx only


Manufactured by OMJ Pharmaceuticals, Inc.,

San Germán, P.R. 00683

for Novartis Ophthalmics

Duluth, GA 30097


March, 2001

carbachol injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:58768-735
Route of AdministrationINTRAOCULAR
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Carbachol (UNII: 8Y164V895Y) (Carbachol - UNII:8Y164V895Y) 0.1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
calcium chloride dihydrate (UNII: M4I0D6VV5M) 0.481 mg  in 1 mL
hydrochloric acid (UNII: QTT17582CB)  
magnesium chloride hexahydrate (UNII: 02F3473H9O) 0.3 mg  in 1 mL
potassium chloride (UNII: 660YQ98I10) 0.75 mg  in 1 mL
sodium acetate trihydrate (UNII: 4550K0SC9B) 3.9 mg  in 1 mL
Sodium chloride (UNII: 451W47IQ8X) 6.4 mg  in 1 mL
sodium citrate dihydrate (UNII: B22547B95K) 1.7 mg  in 1 mL
sodium hydroxide (UNII: 55X04QC32I)  
water (UNII: 059QF0KO0R)  
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58768-735-1212 in 1 CARTON
11.5 mL in 1 VIAL, GLASS
Labeler - Novartis Ophthalmics

Revised: 9/2006
Document Id: 048AF9C6-4866-4500-9914-CD7071A19B63
Set id: 048AF9C6-4866-4500-9914-CD7071A19B63
Version: 1
Effective Time: 20060919
Novartis Ophthalmics