Methocarbamol

Product NDC
60760-482
11-digit product format
607600482
Labeler code
60760
Product ID
60760-482_b465e8e9-b2a4-0afb-e053-2a95a90a6299
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Methocarbamol
Dosage form
TABLET
Route
ORAL
Labeler
St. Mary's Medical Park Pharmacy
Application
ANDA090200
Marketing category
ANDA
Marketing start
2020-11-18
Marketing end
0000-00-00
Substance
METHOCARBAMOL
Active strength
500 mg/1
Pharmacologic classes
Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60760-482-902025-01-03C16284748780-1f386c649-a431-0266-e053-dadaa90a7c1ab465e6fc-20ff-192d-e053-2a95a90a3f44
60760-482-902023-01-30C16284748780-1f386c649-a431-0266-e053-dadaa90a7c1ab465e6fc-20ff-192d-e053-2a95a90a3f44

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
60760-482-90EA - Each60760-482400098f6-b57c-4164-997f-c2ea3f22b37312021-01-08

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
60760-482-906076004829090 TABLET in 1 BOTTLE, PLASTIC (60760-482-90) 90 tablet2020-11-180000-00-00NoNoCurrent