Methocarbamol

Product NDC
50090-1781
11-digit product format
500901781
Labeler code
50090
Product ID
50090-1781_ee81560c-8542-4384-ae20-9c7ab551c957
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Methocarbamol
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA090200
Marketing category
ANDA
Marketing start
2013-03-20
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 formatDescriptionUnitsMarketing startSampleExclude flagStatus
50090-1781-05009017810020 TABLET in 1 BOTTLE (50090-1781-0) 20 tablet2015-04-16NoNoHistorical
50090-1781-15009017810140 TABLET in 1 BOTTLE (50090-1781-1) 40 tablet2015-04-16NoNoHistorical
50090-1781-25009017810228 TABLET in 1 BOTTLE (50090-1781-2) 28 tablet2015-04-16NoNoHistorical
50090-1781-35009017810330 TABLET in 1 BOTTLE (50090-1781-3) 30 tablet2015-04-16NoNoHistorical
50090-1781-45009017810460 TABLET in 1 BOTTLE (50090-1781-4) 60 tablet2015-04-16NoNoHistorical
50090-1781-650090178106100 TABLET in 1 BOTTLE (50090-1781-6) 100 tablet2020-03-02NoNoHistorical
50090-1781-75009017810712 TABLET in 1 BOTTLE (50090-1781-7) 12 tablet2015-04-16NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Methocarbamol Tablets USP Rx OnlyA-S Medication Solutions2024-01-05HUMAN PRESCRIPTION DRUG LABEL14