Cromolyn Sodium (NuCare Pharmaceuticals, Inc.)
Welcome to the PulseAid listing for the Cromolyn Sodium drug offered from NuCare Pharmaceuticals, Inc.. This Decreased Histamine Release [PE],Mast Cell Stabilizer [EPC] 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: | NuCare Pharmaceuticals, Inc. |
NON-PROPRIETARY NAME: | cromolyn sodium |
SUBSTANCE NAME: | CROMOLYN SODIUM |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Decreased Histamine Release [PE],Mast Cell Stabilizer [EPC] |
ROUTE: | OPHTHALMIC |
DOSAGE FORM: | SOLUTION/ DROPS |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 1995-01-30 |
END MARKETING DATE: | 0000-00-00 |
Cromolyn Sodium HUMAN PRESCRIPTION DRUG Details:
Item Description | Cromolyn Sodium from NuCare Pharmaceuticals, Inc. |
LABELER NAME: | NuCare Pharmaceuticals, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 40(mg/mL) |
START MARKETING DATE: | 1995-01-30 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 68071-3231_51ca74fe-3364-65dc-e054-00144ff88e88 |
PRODUCT NDC: | 68071-3231 |
APPLICATION NUMBER: | ANDA074443 |
Other CROMOLYN SODIUM Pharmaceutical Manufacturers / Labelers: