NDC 68788-7973 – Methocarbamol

Methocarbamol 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-7973

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
Preferred Pharmaceuticals, Inc
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040489
Marketed since
July 28, 2021
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
68788-7973-330 TABLET in 1 BOTTLE (68788-7973-3)Jul 28, 2021
68788-7973-660 TABLET in 1 BOTTLE (68788-7973-6)Jul 28, 2021
68788-7973-990 TABLET in 1 BOTTLE (68788-7973-9)Jul 28, 2021

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