Promethazine Hydrochloride NDC 43063-874

Product information

Brand name (proprietary)

Promethazine Hydrochloride

Generic name (nonproprietary)

promethazine hydrochloride

Active ingredients

Promethazine hydrochloride — 25 mg/1

Dosage form

Tablet

Route

Oral

Labeler

PD-Rx Pharmaceuticals, Inc.

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 040712

Marketing start

Jul 31, 2006

Listing expires

Dec 31, 2027

Other FDA classes

Phenothiazines (Chemical structure)

Identifiers

Product ID 43063-874_526a6362-0f9a-d536-e063-6394a90a5fd0SPL ID 526a6362-0f9a-d536-e063-6394a90a5fd0SPL set ID 5ce082e9-13eb-4e63-a9e2-657d3ef0e9f8RxCUI 992447UNII R61ZEH7I1IUPC 0343063874011

Pharmacologic class

Phenothiazine

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

N443063087401 followed by a unit qualifier and the quantity Copy

Package 43063-0874-01. 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

Other NDCs under ANDA 040712

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