NDC 72887-873

methocarbamol 1000 mg tablet, film coated

On the label: FH2 Pharma LLC.

Where it's made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants FH2 Pharma LLC names for other drugs.

Product details

Generic drug
Methocarbamol: every company that makes it
Form
tablet, film coated, oral
Strength
1000 mg
Approval
ANDA ANDA212707
On the market since
Aug 30, 2024
Package NDCs
72887-873-03
Official label
DailyMed (National Library of Medicine), updated Feb 6, 2025

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