Guanidine hydrochloride (Merck Sharp & Dohme Corp.)
Welcome to the PulseAid listing for the Guanidine hydrochloride drug offered from Merck Sharp & Dohme Corp.. This Acetylcholine Releasing Agent [EPC],Increased Acetylcholine Activity [PE] 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: | Merck Sharp & Dohme Corp. |
| NON-PROPRIETARY NAME: | Guanidine hydrochloride |
| SUBSTANCE NAME: | GUANIDINE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Acetylcholine Releasing Agent [EPC],Increased Acetylcholine Activity [PE] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 1939-10-02 |
| END MARKETING DATE: | 0000-00-00 |
Guanidine hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Guanidine hydrochloride from Merck Sharp & Dohme Corp. |
| LABELER NAME: | Merck Sharp & Dohme Corp. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 125(mg/1) |
| START MARKETING DATE: | 1939-10-02 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0085-0492_99865db3-d499-4f5b-83d0-4c0363a66c8a |
| PRODUCT NDC: | 0085-0492 |
| APPLICATION NUMBER: | NDA001546 |
Other GUANIDINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
