Cyclopentolate Hydrochloride (Bausch & Lomb Incorporated)


Welcome to the PulseAid listing for the Cyclopentolate Hydrochloride drug offered from Bausch & Lomb Incorporated. This pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: Bausch & Lomb Incorporated
NON-PROPRIETARY NAME: Cyclopentolate Hydrochloride
SUBSTANCE NAME: CYCLOPENTOLATE HYDROCHLORIDE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS:
ROUTE: OPHTHALMIC
DOSAGE FORM: SOLUTION/ DROPS
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 1994-04-29
END MARKETING DATE: 0000-00-00


Cyclopentolate Hydrochloride HUMAN PRESCRIPTION DRUG Details:

Item DescriptionCyclopentolate Hydrochloride from Bausch & Lomb Incorporated
LABELER NAME: Bausch & Lomb Incorporated
DEA SCHEDULE:
ACTIVE STRENGTH: 10(mg/mL)
START MARKETING DATE: 1994-04-29
END MARKETING DATE: 0000-00-00
PRODUCT ID: 24208-735_eebb54c8-12ba-4534-8918-93a770b5e67f
PRODUCT NDC: 24208-735
APPLICATION NUMBER: ANDA040075

Other CYCLOPENTOLATE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Akorn, Inc.Cyclopentolate
Alcon Laboratories, Inc.Cyclogyl
Bausch & Lomb IncorporatedCyclopentolate Hydrochloride
Physicians Total Care, Inc.Cyclopentolate Hydrochloride
Rebel Distributors CorpCyclopentolate Hydrochloride
Rebel Distributors Corp.AK-PENTOLATE
Sandoz Inc.Cyclopentolate Hydrochloride