Propranolol Scopolamine is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Tps. The primary component is Scopolamine Hydrobromide; Propranolol Hydrochloride.
| Product ID | 69267-201_0579a12e-690c-3fa0-e054-00144ff88e88 |
| NDC | 69267-201 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Propranolol Scopolamine |
| Generic Name | Propranolol Scopolamine |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2014-10-01 |
| Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
| Labeler Name | TPS |
| Substance Name | SCOPOLAMINE HYDROBROMIDE; PROPRANOLOL HYDROCHLORIDE |
| Active Ingredient Strength | 0 mg/20.25mg; mg/20.25mg |
| Pharm Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Anticholinergic [EPC],Cholinergic Antagonists [MoA] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 2014-10-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2014-10-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2014-10-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2014-10-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2014-10-01 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| SCOPOLAMINE HYDROBROMIDE | .25 mg/20.25mg |
| SPL SET ID: | 0579a12e-690b-3fa0-e054-00144ff88e88 |
| Manufacturer | |
| UNII |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 69267-201 | Propranolol Scopolamine | Propranolol Scopolamine |
| 69267-202 | Propranolol Scopolamine | Propranolol Scopolamine |