Methocarbamol NDC 60760-875

Product information

Brand name (proprietary)

Methocarbamol

Generic name (nonproprietary)

methocarbamol

Active ingredients

Methocarbamol — 750 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

Jul 7, 2026

Listing expires

Dec 31, 2027

Other FDA classes

Centrally-mediated Muscle Relaxation (Physiologic effect)

Identifiers

Product ID 60760-875_584e9b94-38ee-8f42-e063-6394a90ac548SPL ID 584e9b94-38ee-8f42-e063-6394a90ac548SPL set ID 56090def-7caf-e916-e063-6294a90a6ac2RxCUI 197944UNII 125OD7737X

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

N460760087528 followed by a unit qualifier and the quantity Copy

Package 60760-0875-28. 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

Other NDCs under ANDA 213967

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