NDC 50742-505
Scopolamine
Scopolamine
Scopolamine is a Transdermal Patch, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Ingenus Pharmaceuticals, Llc. The primary component is Scopolamine.
| Product ID | 50742-505_0b513236-5471-4d8c-bc58-326f674a084b |
| NDC | 50742-505 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Scopolamine |
| Generic Name | Scopolamine |
| Dosage Form | Patch, Extended Release |
| Route of Administration | TRANSDERMAL |
| Marketing Start Date | 2020-11-24 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA212342 |
| Labeler Name | Ingenus Pharmaceuticals, LLC |
| Substance Name | SCOPOLAMINE |
| Active Ingredient Strength | 2 mg/1 |
| Pharm Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |