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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
35356-690-01EA - Each35356-69038597d9d-5b08-4acd-9585-8517f1ca065312013-02-13
35356-690-20EA - Each35356-6904a530900-a97e-498c-bedd-76e63ef44b4212013-02-13
35356-690-30EA - Each35356-6903c806f96-e435-4cf7-a95c-d4c941a51e9712013-02-13
35356-690-40EA - Each35356-690e1979361-be48-44d2-b287-3151bf12273a12013-02-13
35356-690-60EA - Each35356-69043b1061f-b86c-4a09-bf9d-48f8637f1e6412013-02-13
35356-690-90EA - Each35356-6900f3fdf60-c341-4bbe-8b34-620a21fbaf6f12012-07-24