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Scopolamine Hydrobromide
Scopolamine Hydrobromide - 63323-268-01 - (SCOPOLAMINE HYDROBROMIDE)
Drug Information of Scopolamine Hydrobromide
| Product NDC: | 63323-268 |
| Proprietary Name: | Scopolamine Hydrobromide |
| Non Proprietary Name: | SCOPOLAMINE HYDROBROMIDE |
| Active Ingredient(s): | .4 mg/mL & nbsp; SCOPOLAMINE HYDROBROMIDE |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Scopolamine Hydrobromide
| Product NDC: | 63323-268 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20001018 |
Package Information of Scopolamine Hydrobromide
| Package NDC: | 63323-268-01 |
| Package Description: | 25 VIAL, MULTI-DOSE in 1 TRAY (63323-268-01) > 1 mL in 1 VIAL, MULTI-DOSE |
NDC Information of Scopolamine Hydrobromide
| NDC Code | 63323-268-01 |
| Proprietary Name | Scopolamine Hydrobromide |
| Package Description | 25 VIAL, MULTI-DOSE in 1 TRAY (63323-268-01) > 1 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 63323-268 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SCOPOLAMINE HYDROBROMIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 20001018 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | SCOPOLAMINE HYDROBROMIDE |
| Strength Number | .4 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA] |
