Methocarbamol NDC 50090-3578

Product information

Brand name (proprietary)

Methocarbamol

Generic name (nonproprietary)

methocarbamol

Active ingredients

Methocarbamol — 500 mg/1

Dosage form

Tablet, Film coated

Route

Oral

Labeler

A-S Medication Solutions

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 208507

Marketing start

Jan 15, 2018

Listing expires

Dec 31, 2026

Other FDA classes

Centrally-mediated Muscle Relaxation (Physiologic effect)

Identifiers

Product ID 50090-3578_a527bac5-ad4e-4c49-acda-a457ff2ca164SPL ID a527bac5-ad4e-4c49-acda-a457ff2ca164SPL set ID 9357672f-5d4d-40f5-a304-e0c34e174dc3RxCUI 197943UNII 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

N450090357801 followed by a unit qualifier and the quantity Copy

Package 50090-3578-01. 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 208507

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