Tramadol Hydrochloride NDC 69238-2348

Product information

Brand name (proprietary)

Tramadol Hydrochloride

Generic name (nonproprietary)

tramadol hydrochloride

Active ingredients

Tramadol hydrochloride — 50 mg/1

Dosage form

Tablet, Coated

Route

Oral

Labeler

Amneal Pharmaceuticals NY LLC

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 076003

Marketing start

Nov 15, 2010

Listing expires

Dec 31, 2027

DEA schedule

CIV

Other FDA classes

Full Opioid Agonists (Mechanism)

Identifiers

Product ID 69238-2348_267b7da8-2e24-4130-92d5-98d6da176ed6SPL ID 267b7da8-2e24-4130-92d5-98d6da176ed6SPL set ID 67919c2c-2f8a-4bbb-bef5-0cd6c1e63a16RxCUI 835603UNII 9N7R477WCKUPC 0369238234817

Pharmacologic class

Opioid 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

N469238234801 followed by a unit qualifier and the quantity Copy

Package 69238-2348-01. 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

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

Other NDCs under ANDA 076003

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