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Atropine Sulfate
Atropine Sulfate - 0641-6006-10 - (Atropine Sulfate)
Drug Information of Atropine Sulfate
| Product NDC: | 0641-6006 |
| Proprietary Name: | Atropine Sulfate |
| Non Proprietary Name: | Atropine Sulfate |
| Active Ingredient(s): | .4 mg/mL & nbsp; Atropine Sulfate |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Atropine Sulfate
| Product NDC: | 0641-6006 |
| Labeler Name: | West-ward Pharmaceutical Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19710101 |
Package Information of Atropine Sulfate
| Package NDC: | 0641-6006-10 |
| Package Description: | 10 VIAL in 1 CARTON (0641-6006-10) > 20 mL in 1 VIAL (0641-6006-01) |
NDC Information of Atropine Sulfate
| NDC Code | 0641-6006-10 |
| Proprietary Name | Atropine Sulfate |
| Package Description | 10 VIAL in 1 CARTON (0641-6006-10) > 20 mL in 1 VIAL (0641-6006-01) |
| Product NDC | 0641-6006 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Atropine Sulfate |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 19710101 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | West-ward Pharmaceutical Corp. |
| Substance Name | ATROPINE SULFATE |
| Strength Number | .4 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |
