Lorazepam NDC 71610-122

Product information

Brand name (proprietary)

Lorazepam

Generic name (nonproprietary)

lorazepam

Active ingredients

Lorazepam — 1 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 078203

Marketing start

Oct 9, 2009

Listing expires

Dec 31, 2026

DEA schedule

CIV

Other FDA classes

Benzodiazepines (Chemical structure)

Identifiers

Product ID 71610-122_3931aebc-69f6-4756-9ca6-72cec3c18be5SPL ID 3931aebc-69f6-4756-9ca6-72cec3c18be5SPL set ID 8df3eed3-c936-4772-ab08-574c54dd8bf5RxCUI 197901UNII O26FZP769L

Pharmacologic class

Benzodiazepine

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

N471610012210 followed by a unit qualifier and the quantity Copy

Package 71610-0122-10. 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 078203

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

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