Baclofen

Product NDC
63739-974
11-digit product format
637390974
Labeler code
63739
Product ID
63739-974_40a810f3-f69d-433e-a589-377edcf08f1e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
baclofen
Dosage form
TABLET
Route
ORAL
Labeler
McKesson Corporation dba SKY Packaging
Application
ANDA077241
Marketing category
ANDA
Marketing start
2005-12-01
Marketing end
0000-00-00
Substance
BACLOFEN
Active strength
20 mg/1
Pharmacologic classes
GABA A Agonists [MoA],GABA B Agonists [MoA],gamma-Aminobutyric Acid-ergic Agonist [EPC]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63739-974-102020-07-22C16284748780-1ab0e2407-2d12-f274-e053-dbdaa90a647145314bb7-91e5-4cd4-b38a-83097812e6a9

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63739-974-10EA - Each63739-974c9c02266-52b2-4de4-a8df-13e1bd382c1e12015-09-10