NDC Package 70512-032-04 Hydrocortisone Butyrate

View Billable Units, 11-Digit Format, RxNorm

Package Information
Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:

70512-032-04

Package Description:

1 TUBE in 1 CARTON / 118 mL in 1 TUBE

Product Code:

70512-032

Proprietary Name:

Hydrocortisone Butyrate

Usage Information:

This medication is used to treat a variety of skin conditions (e.g., eczema, dermatitis, allergies, rash). Hydrocortisone butyrate reduces the swelling, itching, and redness that can occur in these types of conditions. The topical solution is used to treat severe dandruff (seborrheic dermatitis). This medication is a medium-strength corticosteroid.

11-Digit NDC Billing Format:

70512003204

Billing Unit:

ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.

Labeler Name:

Sola Pharmaceuticals

Sample Package:

FDA Application Number:

ANDA209556

Marketing Category:

ANDA - A product marketed under an approved Abbreviated New Drug Application.

Start Marketing Date:

02-04-2019

End Marketing Date:

12-05-2022

Listing Expiration Date:

12-05-2022

Exclude Flag:

Code Structure:

70512 - Sola Pharmaceuticals
- 70512-032 - Hydrocortisone Butyrate
  - 70512-032-04 - 1 TUBE in 1 CARTON / 118 mL in 1 TUBE

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 70512-032-04?

The NDC Packaged Code 70512-032-04 is assigned to a package of 1 tube in 1 carton / 118 ml in 1 tube of Hydrocortisone Butyrate, labeled by Sola Pharmaceuticals. The product's dosage form is and is administered via form.

Is NDC 70512-032 included in the NDC Directory?

No, Hydrocortisone Butyrate with product code 70512-032 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Sola Pharmaceuticals on February 04, 2019 and its listing in the NDC Directory is set to expire on December 05, 2022 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 70512-032-04?

The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

What is the 11-digit format for NDC 70512-032-04?

The 11-digit format is 70512003204. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	70512-032-04	5-4-2	70512-0032-04

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