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CORGARD
CORGARD - 60793-800-01 - (nadolol)
Drug Information of CORGARD
| Product NDC: | 60793-800 |
| Proprietary Name: | CORGARD |
| Non Proprietary Name: | nadolol |
| Active Ingredient(s): | 20 mg/1 & nbsp; nadolol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CORGARD
| Product NDC: | 60793-800 |
| Labeler Name: | King Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018063 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19791210 |
Package Information of CORGARD
| Package NDC: | 60793-800-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (60793-800-01) |
NDC Information of CORGARD
| NDC Code | 60793-800-01 |
| Proprietary Name | CORGARD |
| Package Description | 100 TABLET in 1 BOTTLE (60793-800-01) |
| Product NDC | 60793-800 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | nadolol |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19791210 |
| Marketing Category Name | NDA |
| Labeler Name | King Pharmaceuticals, Inc. |
| Substance Name | NADOLOL |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
