Cromolyn Sodium (Bausch & Lomb Incorporated)
Welcome to the PulseAid listing for the Cromolyn Sodium drug offered from Bausch & Lomb Incorporated. This pharmaceutical is classified as a HUMAN OTC 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 OTC DRUG drug type category.
LABELER NAME / MANUFACTURER: | Bausch & Lomb Incorporated |
NON-PROPRIETARY NAME: | Cromolyn Sodium |
SUBSTANCE NAME: | CROMOLYN SODIUM |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | NASAL |
DOSAGE FORM: | SPRAY, METERED |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2001-07-03 |
END MARKETING DATE: | 0000-00-00 |
Cromolyn Sodium HUMAN OTC DRUG Details:
Item Description | Cromolyn Sodium from Bausch & Lomb Incorporated |
LABELER NAME: | Bausch & Lomb Incorporated |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 5.2(mg/mL) |
START MARKETING DATE: | 2001-07-03 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 57782-397_feb9903f-0958-4e25-ae86-72098a33699c |
PRODUCT NDC: | 57782-397 |
APPLICATION NUMBER: | ANDA075702 |
Other CROMOLYN SODIUM Pharmaceutical Manufacturers / Labelers: