Product NDC: | 76329-3339 |
Proprietary Name: | Atropine Sulfate |
Non Proprietary Name: | Atropine Sulfate |
Active Ingredient(s): | .1 mg/mL & nbsp; Atropine Sulfate |
Administration Route(s): | PARENTERAL |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76329-3339 |
Labeler Name: | International Medication Systems, Limited |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20000601 |
Package NDC: | 76329-3339-1 |
Package Description: | 10 SYRINGE in 1 CARTON (76329-3339-1) > 10 mL in 1 SYRINGE |
NDC Code | 76329-3339-1 |
Proprietary Name | Atropine Sulfate |
Package Description | 10 SYRINGE in 1 CARTON (76329-3339-1) > 10 mL in 1 SYRINGE |
Product NDC | 76329-3339 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Atropine Sulfate |
Dosage Form Name | INJECTION |
Route Name | PARENTERAL |
Start Marketing Date | 20000601 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | International Medication Systems, Limited |
Substance Name | ATROPINE SULFATE |
Strength Number | .1 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |