NDC00172-3966-80: DIPHENOXYLATE HYDROCHLORIDE AND.
DIPHENOXYLATE HYDROCHLORIDE AND. Key specifications include primary_container_type: BOTTLE, medical_designation_and_grade: UNITED STATES PHARMACOPEIA, primary_container_content_quantity: 1000.000 TABLETS, controlled_substance_classification: SCHEDULE V, active_medicament_medicinal_strength: 0.025 MILLIGRAMS ATROPINE SULFATE ACTIVE INGREDIENT AND 2.500 MILLIGRAMS DIPHENOXYLATE HYDROCHLORIDE ACTIVE INGREDIENT, part_name_assigned_by_controlling_agency: DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE TABLETS USP (1) BOTTLE (1000) TABLETS PER BOTTLE. This part is cataloged in the U.S.
Government catalog under NSN 6505-01-042-9261, indicating validated use in U.S. government and defense logistics supply chains. Available through authorized enterprise resellers and TPM (Third Party Maintenance) channels.
Verify compatibility with your specific system configuration before ordering.
| primary_container_type | BOTTLE |
| medical_designation_and_grade | UNITED STATES PHARMACOPEIA |
| primary_container_content_quantity | 1000.000 TABLETS |
| controlled_substance_classification | SCHEDULE V |
| active_medicament_medicinal_strength | 0.025 MILLIGRAMS ATROPINE SULFATE ACTIVE INGREDIENT AND 2.500 MILLIGRAMS DIPHENOXYLATE HYDROCHLORIDE ACTIVE INGREDIENT |
| part_name_assigned_by_controlling_agency | DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE TABLETS USP (1) BOTTLE (1000) TABLETS PER BOTTLE |
| american_hospital_formulary_service_classification_number | 560800 |
| NSN | 6505-01-042-9261 |
| CONTROLLED SUBSTANCE CLASSIFICATION | SCHEDULE V |
| PRIMARY CONTAINER CONTENT QUANTITY | 1000.000 TABLETS |
| MEDICAL DESIGNATION AND GRADE | UNITED STATES PHARMACOPEIA |
| PRIMARY CONTAINER TYPE | BOTTLE |
| PART NAME ASSIGNED BY CONTROLLING AGENCY | DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE TABLETS USP (1) BOTTLE (1000) TABLETS PER BOTTLE |
| AMERICAN HOSPITAL FORMULARY SERVICE CLASSIFICATION NUMBER | 560800 |
| ACTIVE MEDICAMENT MEDICINAL STRENGTH | 0.025 MILLIGRAMS ATROPINE SULFATE ACTIVE INGREDIENT AND 2.500 MILLIGRAMS DIPHENOXYLATE HYDROCHLORIDE ACTIVE INGREDIENT |