NDC 68788-8172 – Methocarbamol

Methocarbamol 750 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC68788-8172

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol Tablets
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA209312
Marketed since
April 25, 2022
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
68788-8172-330 TABLET, COATED in 1 BOTTLE (68788-8172-3)Apr 25, 2022
68788-8172-660 TABLET, COATED in 1 BOTTLE (68788-8172-6)Apr 25, 2022
68788-8172-990 TABLET, COATED in 1 BOTTLE (68788-8172-9)Apr 25, 2022

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