Finasteride
- Product NDC
- 58517-200
- 11-digit product format
- 585170200
- Labeler code
- 58517
- Product ID
- 58517-200_17f863dd-1b47-4f2c-8893-fb06e09250ca
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Finasteride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- New Horizon Rx Group, LLC
- Application
- ANDA090121
- Marketing category
- ANDA
- Marketing start
- 2013-08-13
- Marketing end
- 0000-00-00
- Substance
- FINASTERIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- 5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 58517-200-30 | Finasteride | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 5 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| FINASTERIDE | ACTIVE INGREDIENT | 57GNO57U7G | FINASTERIDE TABLET, FILM COATED [NEW HORIZON RX GROUP, LLC] | 5 | |
| FINASTERIDE | ACTIVE MOIETY | 57GNO57U7G | FINASTERIDE TABLET, FILM COATED [NEW HORIZON RX GROUP, LLC] | 5 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | FINASTERIDE TABLET, FILM COATED [NEW HORIZON RX GROUP, LLC] | 5 | |
| FD&C BLUE NO. 2 | INACTIVE INGREDIENT | L06K8R7DQK | FINASTERIDE TABLET, FILM COATED [NEW HORIZON RX GROUP, LLC] | 5 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | FINASTERIDE TABLET, FILM COATED [NEW HORIZON RX GROUP, LLC] | 5 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | FINASTERIDE TABLET, FILM COATED [NEW HORIZON RX GROUP, LLC] | 5 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | FINASTERIDE TABLET, FILM COATED [NEW HORIZON RX GROUP, LLC] | 5 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | FINASTERIDE TABLET, FILM COATED [NEW HORIZON RX GROUP, LLC] | 5 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | FINASTERIDE TABLET, FILM COATED [NEW HORIZON RX GROUP, LLC] | 5 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | FINASTERIDE TABLET, FILM COATED [NEW HORIZON RX GROUP, LLC] | 5 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | FINASTERIDE TABLET, FILM COATED [NEW HORIZON RX GROUP, LLC] | 5 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 58517-200 | FINASTERIDE TABLET, FILM COATED [NEW HORIZON RX GROUP, LLC] | 5 | Legacy NDC, 1 package rows | 20140101_be68c512-7985-47fa-a64b-6bac80bd9751.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 58517-200-30 | 58517020030 | 30 in 1 BOTTLE | Historical |