Bicalutamide

Product NDC
0093-0220
11-digit product format
000930220
Labeler code
0093
Product ID
0093-0220_2975092d-62bd-4e74-ba3a-d20bd47a1b7a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Bicalutamide
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Teva Pharmaceuticals USA, Inc.
Application
ANDA076932
Marketing category
ANDA
Marketing start
2009-07-06
Marketing end
2019-10-31
Substance
BICALUTAMIDE
Active strength
50 mg/1
Pharmacologic classes
Androgen Receptor Antagonists [MoA],Androgen Receptor Inhibitor [EPC]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
18edadb0-25ee-467f-798d-437ee65ee754Product name320150616

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0093-0220-01EA - Each0093-02205ba19630-78a7-4ea6-8359-49acc145e58512012-07-24
0093-0220-56EA - Each0093-022004b691a6-0c6d-40f7-9b6d-b5d631e760ea12012-07-24

DailyMed Socrata Ingredients#

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
199123bicalutamide 50 MG Oral TabletPSN020d34eb-9560-4218-9d87-dfdeff705c3a1
199123bicalutamide 50 MG Oral TabletSCD020d34eb-9560-4218-9d87-dfdeff705c3a1