Methocarbamol

Product NDC
86211-114
11-digit product format
862110114
Labeler code
86211
Product ID
86211-114_f0d0d131-38fa-4644-bfc9-d027b3511149
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Methocarbamol
Dosage form
INJECTION
Route
INTRAMUSCULAR; INTRAVENOUS; INTRAVENOUS
Labeler
JVET PHARMACEUTICALS LLC
Application
ANDA211504
Marketing category
ANDA
Marketing start
2026-05-22
Substance
METHOCARBAMOL
Active strength
100 mg/mL
Pharmacologic classes
Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Methocarbamol
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
METHOCARBAMOL100 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii125OD7737X
Rxcui238175

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
492965be-47bc-38cf-57c4-5c5e0343abe5Product name620211028
02a01e9c-3f4e-c0ee-6542-be865127aea3Product name820190205

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
86211-114-01Methocarbamol10 mL in 1 VIALINJECTION101
86211-114-10Methocarbamol10 in 1 CARTONINJECTION101

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
238175methocarbamol 1000 MG in 10 ML InjectionPSNd9e4748f-11c5-4d87-b260-1be94febe8061
23817510 ML methocarbamol 100 MG/ML InjectionSCDd9e4748f-11c5-4d87-b260-1be94febe8061
238175methocarbamol 1000 MG per 10 ML InjectionSYd9e4748f-11c5-4d87-b260-1be94febe8061

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
86211-114-018621101140110 mL in 1 VIAL10 mlHistorical
86211-114-108621101141010 VIAL in 1 CARTON (86211-114-10) / 10 mL in 1 VIAL (86211-114-01) 10 vial2026-05-22NoNoHistorical