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SECTRAL
SECTRAL - 67857-700-01 - (acebutolol hydrochloride)
Drug Information of SECTRAL
| Product NDC: | 67857-700 |
| Proprietary Name: | SECTRAL |
| 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 SECTRAL
| Product NDC: | 67857-700 |
| Labeler Name: | Promius Pharma, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018917 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19841228 |
Package Information of SECTRAL
| Package NDC: | 67857-700-01 |
| Package Description: | 100 CAPSULE in 1 BOTTLE, PLASTIC (67857-700-01) |
NDC Information of SECTRAL
| NDC Code | 67857-700-01 |
| Proprietary Name | SECTRAL |
| Package Description | 100 CAPSULE in 1 BOTTLE, PLASTIC (67857-700-01) |
| Product NDC | 67857-700 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | acebutolol hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19841228 |
| Marketing Category Name | NDA |
| Labeler Name | Promius Pharma, LLC |
| Substance Name | ACEBUTOLOL HYDROCHLORIDE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
