| NDC Code | 51662-1339-1 |
|---|
| Package Description | 1 mL in 1 VIAL, SINGLE-DOSE (51662-1339-1) |
|---|
| Product NDC | 51662-1339 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Atropine Sulfate |
|---|
| Non-Proprietary Name | Atropine Sulfate |
|---|
| Dosage Form | INJECTION, SOLUTION |
|---|
| Usage | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
|---|
| Start Marketing Date | 20181221 |
|---|
| Marketing Category Name | UNAPPROVED DRUG OTHER |
|---|
| Manufacturer | HF Acquisition Co LLC, DBA HealthFirst |
|---|
| Substance Name | ATROPINE SULFATE |
|---|
| Strength | .4 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Anticholinergic [EPC], Cholinergic Antagonists [MoA], Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA] |
|---|