HumulinN (Eli Lilly and Company)
Welcome to the PulseAid listing for the Humulin drug offered from Eli Lilly and Company. 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: | Eli Lilly and Company |
NON-PROPRIETARY NAME: | Insulin human |
SUBSTANCE NAME: | INSULIN HUMAN |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | SUBCUTANEOUS |
DOSAGE FORM: | INJECTION, SUSPENSION |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 1983-06-27 |
END MARKETING DATE: | 0000-00-00 |
Humulin N HUMAN OTC DRUG Details:
Item Description | Humulin N from Eli Lilly and Company |
LABELER NAME: | Eli Lilly and Company |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 100([iU]/mL) |
START MARKETING DATE: | 1983-06-27 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0002-8315_96565fb7-dbd9-4048-96a7-73e9c3626f6e |
PRODUCT NDC: | 0002-8315 |
APPLICATION NUMBER: | NDA018781 |
Other INSULIN HUMAN Pharmaceutical Manufacturers / Labelers: