Cyclopentolate Hydrochloride (Akorn, Inc.)


Welcome to the PulseAid listing for the Cyclopentolate Hydrochloride drug offered from Akorn, Inc.. 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: Akorn, Inc.
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: 1997-01-13
END MARKETING DATE: 0000-00-00


Cyclopentolate Hydrochloride HUMAN PRESCRIPTION DRUG Details:

Item DescriptionCyclopentolate Hydrochloride from Akorn, Inc.
LABELER NAME: Akorn, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 20(mg/mL)
START MARKETING DATE: 1997-01-13
END MARKETING DATE: 0000-00-00
PRODUCT ID: 17478-097_4b3e7b47-d9d2-4c12-afb5-d42e2247608e
PRODUCT NDC: 17478-097
APPLICATION NUMBER: ANDA040165

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