NDC 61919-616 – Methocarbamol

Methocarbamol 750 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC61919-616

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
DIRECT RX
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA209312
Marketed since
April 18, 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
61919-616-2020 TABLET, COATED in 1 BOTTLE (61919-616-20)Apr 18, 2019
61919-616-3030 TABLET, COATED in 1 BOTTLE (61919-616-30)Apr 18, 2019
61919-616-6060 TABLET, COATED in 1 BOTTLE (61919-616-60)Apr 18, 2019

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