Lanolin (Dynarex Corporation)
Welcome to the PulseAid listing for the Lanolin drug offered from Dynarex Corporation. 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: | Dynarex Corporation |
NON-PROPRIETARY NAME: | Lanolin |
SUBSTANCE NAME: | LANOLIN |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | OINTMENT |
MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
START MARKETING DATE: | 2010-05-12 |
END MARKETING DATE: | 0000-00-00 |
Lanolin HUMAN OTC DRUG Details:
Item Description | Lanolin from Dynarex Corporation |
LABELER NAME: | Dynarex Corporation |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 50(g/100g) |
START MARKETING DATE: | 2010-05-12 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 67777-232_a2902a28-599d-4c10-8a0c-957b4bed94f2 |
PRODUCT NDC: | 67777-232 |
APPLICATION NUMBER: | part347 |
Other LANOLIN Pharmaceutical Manufacturers / Labelers: