up and up hair regrowth treatment for women NDC 11673-919

Product information

Brand name (proprietary)

up and up hair regrowth treatment for women

Generic name (nonproprietary)

minoxidil

Active ingredients

Minoxidil — 2 g/100mL

Dosage form

Solution

Route

Topical

Labeler

Target Corporation

Product type

Over-the-counter drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 075357

Marketing start

Jan 5, 2022

Listing expires

Dec 31, 2026

Other FDA classes

Arteriolar Vasodilation (Physiologic effect)

Identifiers

Product ID 11673-919_bfaa2972-f71d-42c2-b3ec-2294efb5bed3SPL ID bfaa2972-f71d-42c2-b3ec-2294efb5bed3SPL set ID e1211429-46da-4824-9471-c421dae79d24RxCUI 311723UNII 5965120SH1

Pharmacologic class

Arteriolar Vasodilator

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N411673091930 followed by a unit qualifier and the quantity Copy

Package 11673-0919-30. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 075357

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.