Home
>
National Drug Code (NDC)
>
Acebutolol Hydrochloride
Acebutolol Hydrochloride - 65162-669-50 - (Acebutolol Hydrochloride)
Drug Information of Acebutolol Hydrochloride
| Product NDC: | 65162-669 |
| Proprietary Name: | Acebutolol Hydrochloride |
| Non Proprietary Name: | Acebutolol Hydrochloride |
| Active Ingredient(s): | 200 mg/1 & nbsp; Acebutolol Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Acebutolol Hydrochloride
| Product NDC: | 65162-669 |
| Labeler Name: | Amneal Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075047 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091201 |
Package Information of Acebutolol Hydrochloride
| Package NDC: | 65162-669-50 |
| Package Description: | 500 CAPSULE in 1 BOTTLE (65162-669-50) |
NDC Information of Acebutolol Hydrochloride
| NDC Code | 65162-669-50 |
| Proprietary Name | Acebutolol Hydrochloride |
| Package Description | 500 CAPSULE in 1 BOTTLE (65162-669-50) |
| Product NDC | 65162-669 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Acebutolol Hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20091201 |
| Marketing Category Name | ANDA |
| Labeler Name | Amneal Pharmaceuticals, LLC |
| Substance Name | ACEBUTOLOL HYDROCHLORIDE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
