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Nymalize
Nymalize - 24338-200-16 - (nimodipine)
Drug Information of Nymalize
| Product NDC: | 24338-200 |
| Proprietary Name: | Nymalize |
| Non Proprietary Name: | nimodipine |
| Active Ingredient(s): | 60 mg/20mL & nbsp; nimodipine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nymalize
| Product NDC: | 24338-200 |
| Labeler Name: | Arbor Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA203340 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130603 |
Package Information of Nymalize
| Package NDC: | 24338-200-16 |
| Package Description: | 473 mL in 1 BOTTLE (24338-200-16) |
NDC Information of Nymalize
| NDC Code | 24338-200-16 |
| Proprietary Name | Nymalize |
| Package Description | 473 mL in 1 BOTTLE (24338-200-16) |
| Product NDC | 24338-200 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | nimodipine |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20130603 |
| Marketing Category Name | NDA |
| Labeler Name | Arbor Pharmaceuticals |
| Substance Name | NIMODIPINE |
| Strength Number | 60 |
| Strength Unit | mg/20mL |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |
