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PROPRANOLOL
PROPRANOLOL - 16590-808-30 - (PROPRANOLOL HYDROCHLORIDE)
Drug Information of PROPRANOLOL
| Product NDC: | 16590-808 |
| Proprietary Name: | PROPRANOLOL |
| Non Proprietary Name: | PROPRANOLOL HYDROCHLORIDE |
| Active Ingredient(s): | 10 mg/1 & nbsp; PROPRANOLOL HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PROPRANOLOL
| Product NDC: | 16590-808 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA070175 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19860101 |
Package Information of PROPRANOLOL
| Package NDC: | 16590-808-30 |
| Package Description: | 30 TABLET in 1 BOTTLE, PLASTIC (16590-808-30) |
NDC Information of PROPRANOLOL
| NDC Code | 16590-808-30 |
| Proprietary Name | PROPRANOLOL |
| Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (16590-808-30) |
| Product NDC | 16590-808 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PROPRANOLOL HYDROCHLORIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19860101 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT RX USA LLC |
| Substance Name | PROPRANOLOL HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
