Methocarbamol

Product NDC
63629-4422
11-digit product format
636294422
Labeler code
63629
Product ID
63629-4422_2a688115-8e10-4313-8598-821b523af21d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
methocarbamol
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA040489
Marketing category
ANDA
Marketing start
2003-01-29
Marketing end
0000-00-00
Substance
METHOCARBAMOL
Active strength
750 mg/1
Pharmacologic classes
Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63629-4422-12020-07-06C16284748780-19d75b9d0-b782-f424-e053-dadaa90a57ce0149c87b-c18b-4f64-8baa-a16e54cebd9d
63629-4422-12020-01-31C16284748780-19d75b9d0-b782-f424-e053-dadaa90a57ce0149c87b-c18b-4f64-8baa-a16e54cebd9d