Bupropion Hydrochloride NDC 71610-899

Product information

Brand name (proprietary)

Bupropion Hydrochloride

Generic name (nonproprietary)

bupropion hydrochloride

Active ingredients

Bupropion hydrochloride — 75 mg/1

Dosage form

Tablet

Route

Oral

Labeler

Aphena Pharma Solutions - Tennessee, LLC

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 206975

Marketing start

Jan 30, 2025

Listing expires

Dec 31, 2027

Other FDA classes

Dopamine Uptake Inhibitors (Mechanism)Increased Dopamine Activity (Physiologic effect)Increased Norepinephrine Activity (Physiologic effect)Norepinephrine Uptake Inhibitors (Mechanism)

Identifiers

Product ID 71610-899_59d3655a-a828-6c81-e063-6294a90ac103SPL ID 59d3655a-a828-6c81-e063-6294a90ac103SPL set ID 334e5635-e4cc-cf2a-e063-6294a90ae1e1RxCUI 993691UNII ZG7E5POY8O

Pharmacologic class

Aminoketone

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

N471610089942 followed by a unit qualifier and the quantity Copy

Package 71610-0899-42. 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 206975

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