Pseudoephedrine Hydrochloride NDC 21130-204

Product information

Brand name (proprietary)

Pseudoephedrine Hydrochloride

Generic name (nonproprietary)

pseudoephedrine hydrochloride

Active ingredients

Pseudoephedrine hydrochloride — 120 mg/1

Dosage form

Tablet, Film coated, Extended release

Route

Oral

Labeler

Safeway Inc.

Product type

Over-the-counter drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 077442

Marketing start

Apr 28, 2006

Listing expires

Dec 31, 2026

Other FDA classes

Adrenergic alpha-Agonists (Mechanism)

Identifiers

Product ID 21130-204_22744b1f-71f8-4db8-b2d5-1da1ea2a452aSPL ID 22744b1f-71f8-4db8-b2d5-1da1ea2a452aSPL set ID 01a5d9dd-f123-443b-b968-412c0aadaaa2RxCUI 1049154UNII 6V9V2RYJ8N

Pharmacologic class

alpha-Adrenergic Agonist

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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N421130020421 followed by a unit qualifier and the quantity Copy

Package 21130-0204-21. 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 077442

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