NDC 0006-0072
PROSCAR
Finasteride
PROSCAR is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Merck Sharp & Dohme Corp.. The primary component is Finasteride.
| Product ID | 0006-0072_24a8b69a-45b6-4064-96d2-3279c6a1fb7a |
| NDC | 0006-0072 |
| Product Type | Human Prescription Drug |
| Proprietary Name | PROSCAR |
| Generic Name | Finasteride |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 1992-06-19 |
| Marketing Category | NDA / NDA |
| Application Number | NDA020180 |
| Labeler Name | Merck Sharp & Dohme Corp. |
| Substance Name | FINASTERIDE |
| Active Ingredient Strength | 5 mg/1 |
| Pharm Classes | 5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |
Packaging
NDC 0006-0072-31
30 TABLET, FILM COATED in 1 BOTTLE (0006-0072-31)
| Marketing Start Date | 1992-06-19 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 0006-0072-31 [00006007231]
PROSCAR TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA020180 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1992-06-19 |
NDC 0006-0072-82 [00006007282]
PROSCAR TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA020180 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1992-06-19 |
| Marketing End Date | 2010-07-19 |
NDC 0006-0072-28 [00006007228]
PROSCAR TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA020180 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1992-06-19 |
| Marketing End Date | 2010-07-19 |
NDC 0006-0072-01 [00006007201]
PROSCAR TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA020180 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1992-06-19 |
| Marketing End Date | 2010-07-19 |
NDC 0006-0072-58 [00006007258]
PROSCAR TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA020180 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1992-06-19 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| FINASTERIDE | 5 mg/1 |
OpenFDA Data
| SPL SET ID: | 7c01f541-1c88-400c-41a9-7cbb9dee50c0 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
Pharmacological Class
- 5-alpha Reductase Inhibitor [EPC]
- 5-alpha Reductase Inhibitors [MoA]
NDC Crossover Matching brand name "PROSCAR" or generic name "Finasteride"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0006-0072 | PROSCAR | FINASTERIDE |
| 0093-7355 | Finasteride | Finasteride |
| 0179-0175 | Finasteride | Finasteride |
| 0378-5036 | Finasteride | finasteride |
| 0904-6830 | Finasteride | Finasteride |
| 16729-089 | Finasteride | Finasteride |
| 16729-090 | Finasteride | finasteride |
| 17856-0090 | Finasteride | finasteride |
| 31722-525 | Finasteride | Finasteride |
| 31722-526 | Finasteride | Finasteride |
| 33261-833 | Finasteride | Finasteride |
| 35573-400 | Finasteride | Finasteride |
| 42291-280 | Finasteride | Finasteride |
| 43598-303 | Finasteride | Finasteride |
| 43598-390 | Finasteride | Finasteride |
| 45963-500 | Finasteride | Finasteride |
| 45963-600 | FINASTERIDE | FINASTERIDE |
| 47335-714 | Finasteride | Finasteride |
| 47335-715 | FINASTERIDE | FINASTERIDE |
| 50090-1718 | Finasteride | finasteride |
| 0006-0071 | PROPECIA | finasteride |
Trademark Results [PROSCAR]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PROSCAR 73757633 1546049 Live/Registered |
Merck & Co., Inc. 1988-10-14 |
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