Phentermine Hydrochloride NDC 71335-2488

Product information

Brand name (proprietary)

Phentermine Hydrochloride

Generic name (nonproprietary)

phentermine hydrochloride

Active ingredients

Phentermine hydrochloride — 37.5 mg/1

Dosage form

Tablet

Route

Oral

Labeler

Bryant Ranch Prepack

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 200272

Marketing start

Feb 15, 2024

Marketing end

Apr 30, 2028

DEA schedule

CIV

Other FDA classes

Appetite Suppression (Physiologic effect)Increased Sympathetic Activity (Physiologic effect)

Identifiers

Product ID 71335-2488_6738a0d7-aab6-4c1a-8d28-efa24860f432SPL ID 6738a0d7-aab6-4c1a-8d28-efa24860f432SPL set ID e6939fcf-3db2-492a-99ed-a384cdeea7a2RxCUI 803353UNII 0K2I505OTV

Pharmacologic class

Sympathomimetic Amine Anorectic

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

N471335248800 followed by a unit qualifier and the quantity Copy

Package 71335-2488-00. 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 200272

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