Product NDC: | 0548-3339 |
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: | 0548-3339 |
Labeler Name: | Amphastar Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 19900102 |
Package NDC: | 0548-3339-00 |
Package Description: | 10 SYRINGE in 1 PACKAGE (0548-3339-00) > 10 mL in 1 SYRINGE |
NDC Code | 0548-3339-00 |
Proprietary Name | Atropine Sulfate |
Package Description | 10 SYRINGE in 1 PACKAGE (0548-3339-00) > 10 mL in 1 SYRINGE |
Product NDC | 0548-3339 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Atropine Sulfate |
Dosage Form Name | INJECTION |
Route Name | PARENTERAL |
Start Marketing Date | 19900102 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Amphastar Pharmaceuticals, Inc. |
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] |