Methocarbamol

Product NDC
35356-690
11-digit product format
353560690
Labeler code
35356
Product ID
35356-690_b1092311-a2b6-42c0-9f81-ae420731ebda
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
methocarbamol
Dosage form
TABLET
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA040489
Marketing category
ANDA
Marketing start
2003-01-29
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

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
125OD7737XMETHOCARBAMOL532-03-6METHOCARBAMOL