Celecoxib

Product NDC
55700-430
11-digit product format
557000430
Labeler code
55700
Product ID
55700-430_41acc7dc-ce13-4221-ab86-2004ae117b8a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Celecoxib
Dosage form
CAPSULE
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA206827
Marketing category
ANDA
Marketing start
2016-02-01
Marketing end
0000-00-00
Substance
CELECOXIB
Active strength
200 mg/1
Pharmacologic classes
Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55700-430-14EA - Each55700-4302149ba7b-2fa3-4f01-8b7a-d453036e3d8912016-11-08
55700-430-30EA - Each55700-430f6d1e283-0c12-448d-8b78-169f2887136312016-11-08
55700-430-60EA - Each55700-43083943211-a268-4c7c-81d4-08fbb451794712016-11-08