Methocarbamol

Product NDC
71205-097
11-digit product format
712050097
Labeler code
71205
Product ID
71205-097_b112a584-199f-42dd-b6e6-b8fccc63dc85
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Methocarbamol
Dosage form
TABLET
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA085159
Marketing category
ANDA
Marketing start
2000-01-01
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
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71205-097METHOCARBAMOL TABLET [PROFICIENT RX LP]3Legacy NDC20191029_55e97786-765f-4760-88eb-3c403926159e.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71205-097-207120500972020 TABLET in 1 BOTTLE, PLASTIC (71205-097-20) 20 tablet2018-09-040000-00-00NoNoCurrent
71205-097-307120500973030 TABLET in 1 BOTTLE, PLASTIC (71205-097-30) 30 tablet2018-09-040000-00-00NoNoCurrent
71205-097-407120500974040 TABLET in 1 BOTTLE, PLASTIC (71205-097-40) 40 tablet2018-09-040000-00-00NoNoCurrent
71205-097-457120500974545 TABLET in 1 BOTTLE, PLASTIC (71205-097-45) 45 tablet2018-09-040000-00-00NoNoCurrent
71205-097-607120500976060 TABLET in 1 BOTTLE, PLASTIC (71205-097-60) 60 tablet2018-09-040000-00-00NoNoCurrent
71205-097-907120500979090 TABLET in 1 BOTTLE, PLASTIC (71205-097-90) 90 tablet2018-09-040000-00-00NoNoCurrent