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Amlodipine besylate
Amlodipine besylate - 0143-9961-30 - (Amlodipine besylate)
Drug Information of Amlodipine besylate
| Product NDC: | 0143-9961 |
| Proprietary Name: | Amlodipine besylate |
| Non Proprietary Name: | Amlodipine besylate |
| Active Ingredient(s): | 10 mg/1 & nbsp; Amlodipine besylate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Amlodipine besylate
| Product NDC: | 0143-9961 |
| Labeler Name: | West-ward Pharmaceutical Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077771 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110412 |
Package Information of Amlodipine besylate
| Package NDC: | 0143-9961-30 |
| Package Description: | 30 TABLET in 1 BOTTLE (0143-9961-30) |
NDC Information of Amlodipine besylate
| NDC Code | 0143-9961-30 |
| Proprietary Name | Amlodipine besylate |
| Package Description | 30 TABLET in 1 BOTTLE (0143-9961-30) |
| Product NDC | 0143-9961 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Amlodipine besylate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110412 |
| Marketing Category Name | ANDA |
| Labeler Name | West-ward Pharmaceutical Corp |
| Substance Name | AMLODIPINE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |
