NDC 43063-905 – Methocarbamol

Methocarbamol 750 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC43063-905

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol Tablets
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA209312
Marketed since
July 2, 2018
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (5)

Package NDCDescriptionSince
43063-905-1414 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-905-14)Nov 8, 2018
43063-905-2020 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-905-20)Nov 8, 2018
43063-905-3030 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-905-30)Nov 8, 2018
43063-905-4040 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-905-40)Nov 8, 2018
43063-905-6060 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-905-60)Jan 9, 2019

Other Methocarbamol products