Methocarbamol NDC 60760-874

Product information

Brand name (proprietary)

Methocarbamol

Generic name (nonproprietary)

methocarbamol

Active ingredients

Methocarbamol — 500 mg/1

Dosage form

Tablet, Film coated

Route

Oral

Labeler

St. Mary's Medical Park Pharmacy

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 213967

Marketing start

Sep 17, 2026

Listing expires

Dec 31, 2027

Other FDA classes

Centrally-mediated Muscle Relaxation (Physiologic effect)

Identifiers

Product ID 60760-874_5bc71001-809c-9aa1-e063-6294a90a67f2SPL ID 5bc71001-809c-9aa1-e063-6294a90a67f2

Pharmacologic class

Muscle Relaxant

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

N460760087490 followed by a unit qualifier and the quantity Copy

Package 60760-0874-90. 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

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 213967

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