Methocarbamol

Product NDC
71335-2795
11-digit product format
713352795
Labeler code
71335
Product ID
71335-2795_2dfcd0f2-2660-425b-81d9-0035e379e61b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Methocarbamol
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA213967
Marketing category
ANDA
Marketing start
2020-08-12
Substance
METHOCARBAMOL
Active strength
750 mg/1
Pharmacologic classes
Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
125OD7737XMETHOCARBAMOL532-03-6METHOCARBAMOL

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
71335-2795-07133527950014 TABLET, FILM COATED in 1 BOTTLE (71335-2795-0) 2025-10-13NoNoHistorical
71335-2795-17133527950120 TABLET, FILM COATED in 1 BOTTLE (71335-2795-1) 2025-10-13NoNoHistorical
71335-2795-27133527950230 TABLET, FILM COATED in 1 BOTTLE (71335-2795-2) 2025-10-13NoNoHistorical
71335-2795-37133527950340 TABLET, FILM COATED in 1 BOTTLE (71335-2795-3) 2025-10-13NoNoHistorical
71335-2795-471335279504120 TABLET, FILM COATED in 1 BOTTLE (71335-2795-4) 2025-10-13NoNoHistorical
71335-2795-57133527950560 TABLET, FILM COATED in 1 BOTTLE (71335-2795-5) 2025-10-13NoNoHistorical
71335-2795-67133527950690 TABLET, FILM COATED in 1 BOTTLE (71335-2795-6) 2025-10-13NoNoHistorical
71335-2795-771335279507112 TABLET, FILM COATED in 1 BOTTLE (71335-2795-7) 2025-10-13NoNoHistorical
71335-2795-87133527950821 TABLET, FILM COATED in 1 BOTTLE (71335-2795-8) 2025-10-13NoNoHistorical
71335-2795-97133527950984 TABLET, FILM COATED in 1 BOTTLE (71335-2795-9) 2025-10-13NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Methocarbamol Tablets, USP Rx onlyBryant Ranch Prepack2025-10-13HUMAN PRESCRIPTION DRUG LABEL1