Home
>
National Drug Code (NDC)
>
Propranolol Hydrochloride
Propranolol Hydrochloride - 68788-6762-3 - (Propranolol Hydrochloride)
Drug Information of Propranolol Hydrochloride
| Product NDC: | 68788-6762 |
| Proprietary Name: | Propranolol Hydrochloride |
| Non Proprietary Name: | Propranolol Hydrochloride |
| Active Ingredient(s): | 20 mg/1 & nbsp; Propranolol Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Propranolol Hydrochloride
| Product NDC: | 68788-6762 |
| Labeler Name: | Preferred Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078955 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120726 |
Package Information of Propranolol Hydrochloride
| Package NDC: | 68788-6762-3 |
| Package Description: | 30 TABLET in 1 BOTTLE (68788-6762-3) |
NDC Information of Propranolol Hydrochloride
| NDC Code | 68788-6762-3 |
| Proprietary Name | Propranolol Hydrochloride |
| Package Description | 30 TABLET in 1 BOTTLE (68788-6762-3) |
| Product NDC | 68788-6762 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Propranolol Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120726 |
| Marketing Category Name | ANDA |
| Labeler Name | Preferred Pharmaceuticals, Inc. |
| Substance Name | PROPRANOLOL HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
