NDC 60687-568 – Methocarbamol

Methocarbamol 750 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC60687-568

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
American Health Packaging
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090200
Marketed since
May 20, 2020
Marketing end
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (1)

Package NDCDescriptionSince
60687-568-01100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-568-01) / 1 TABLET in 1 BLISTER PACK (60687-568-11)May 20, 2020

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