NDC 0006-0071
PROPECIA
Finasteride
PROPECIA 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 | 0006-0071_263a6fe1-9247-47d5-8396-f35c0dc2081a |
| NDC | 0006-0071 |
| Product Type | Human Prescription Drug |
| Proprietary Name | PROPECIA |
| Generic Name | Finasteride |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 1997-12-19 |
| Marketing Category | NDA / NDA |
| Application Number | NDA020788 |
| Labeler Name | Merck Sharp & Dohme Corp. |
| Substance Name | FINASTERIDE |
| Active Ingredient Strength | 1 mg/1 |
| Pharm Classes | 5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2022-12-31 |
Packaging
NDC 0006-0071-07
1 BLISTER PACK in 1 CARTON (0006-0071-07) > 7 TABLET, FILM COATED in 1 BLISTER PACK
| Marketing Start Date | 1997-12-19 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 0006-0071-54 [00006007154]
PROPECIA TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA020788 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-12-19 |
NDC 0006-0071-61 [00006007161]
PROPECIA TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA020788 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1997-12-19 |
| Marketing End Date | 2010-08-13 |
NDC 0006-0071-31 [00006007131]
PROPECIA TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA020788 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-12-19 |
NDC 0006-0071-07 [00006007107]
PROPECIA TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA020788 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1997-12-19 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| FINASTERIDE | 1 mg/1 |
OpenFDA Data
| SPL SET ID: | 4e07adb4-7807-47d3-b9a9-2332a3047410 |
| 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 "PROPECIA" or generic name "Finasteride"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0006-0071 | PROPECIA | 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 |
| 0006-0072 | PROSCAR | FINASTERIDE |
Trademark Results [PROPECIA]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PROPECIA 79066804 not registered Dead/Abandoned |
ONODA Soushi 2009-02-23 |
 PROPECIA 74660644 2122033 Live/Registered |
MERCK SHARP & DOHME CORP. 1995-04-13 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.