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Dimenhydrinate
Dimenhydrinate - 63323-366-01 - (Dimenhydrinate)
Drug Information of Dimenhydrinate
| Product NDC: | 63323-366 |
| Proprietary Name: | Dimenhydrinate |
| Non Proprietary Name: | Dimenhydrinate |
| Active Ingredient(s): | 50 mg/mL & nbsp; Dimenhydrinate |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dimenhydrinate
| Product NDC: | 63323-366 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040519 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20041129 |
Package Information of Dimenhydrinate
| Package NDC: | 63323-366-01 |
| Package Description: | 25 VIAL in 1 TRAY (63323-366-01) > 1 mL in 1 VIAL |
NDC Information of Dimenhydrinate
| NDC Code | 63323-366-01 |
| Proprietary Name | Dimenhydrinate |
| Package Description | 25 VIAL in 1 TRAY (63323-366-01) > 1 mL in 1 VIAL |
| Product NDC | 63323-366 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dimenhydrinate |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20041129 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | DIMENHYDRINATE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
