Methocarbamol

Product NDC
71610-598
11-digit product format
716100598
Labeler code
71610
Product ID
71610-598_0d749d2c-80a9-4bc4-975e-cd9475de438a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Methocarbamol
Dosage form
TABLET
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Application
ANDA086988
Marketing category
ANDA
Marketing start
1982-01-01
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
71610-598-537161005985360 TABLET in 1 BOTTLE (71610-598-53) 60 tablet2021-09-09NoNoHistorical
71610-598-607161005986090 TABLET in 1 BOTTLE (71610-598-60) 90 tablet2021-09-09NoNoHistorical
71610-598-7071610059870120 TABLET in 1 BOTTLE (71610-598-70) 120 tablet2021-09-09NoNoHistorical
71610-598-8071610059880180 TABLET in 1 BOTTLE (71610-598-80) 180 tablet2021-09-09NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Methocarbamol Tablets, USPAphena Pharma Solutions - Tennessee, LLC2021-11-10HUMAN PRESCRIPTION DRUG LABEL2