NDC 68788-7980 – Methocarbamol

Methocarbamol 750 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-7980

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040489
Marketed since
August 15, 2019
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (3)

Package NDCDescriptionSince
68788-7980-330 TABLET in 1 BOTTLE (68788-7980-3)Aug 15, 2019
68788-7980-660 TABLET in 1 BOTTLE (68788-7980-6)Aug 15, 2019
68788-7980-990 TABLET in 1 BOTTLE (68788-7980-9)Aug 15, 2019

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