Propranolol Hydrochloride and Hydrochlorothiazide is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Mylan Pharmaceuticals Inc.. The primary component is Propranolol Hydrochloride; Hydrochlorothiazide.
| Product ID | 0378-0731_04255a8f-2e83-4ecc-bc5b-6934d53b4913 |
| NDC | 0378-0731 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Propranolol Hydrochloride and Hydrochlorothiazide |
| Generic Name | Propranolol Hydrochloride And Hydrochlorothiazide |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 1987-03-04 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA070947 |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| Substance Name | PROPRANOLOL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE |
| Active Ingredient Strength | 40 mg/1; mg/1 |
| Pharm Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |
| Marketing Start Date | 1987-03-04 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA070947 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1987-03-04 |
| Ingredient | Strength |
|---|---|
| PROPRANOLOL HYDROCHLORIDE | 40 mg/1 |
| SPL SET ID: | 90656b7e-c3b6-46f9-9428-421b7d61d0cc |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0378-0347 | Propranolol Hydrochloride and Hydrochlorothiazide | propranolol hydrochloride and hydrochlorothiazide |
| 0378-0731 | Propranolol Hydrochloride and Hydrochlorothiazide | propranolol hydrochloride and hydrochlorothiazide |