SUPRAX

Product NDC
27437-203
11-digit product format
274370203
Labeler code
27437
Product ID
27437-203_0e44b51b-cba9-4dc5-8ee1-2d151ad24def
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
cefixime
Dosage form
TABLET, CHEWABLE
Route
ORAL
Labeler
Lupin Pharmaceuticals, Inc.
Application
ANDA065380
Marketing category
ANDA
Marketing start
2012-12-05
Marketing end
0000-00-00
Substance
CEFIXIME
Active strength
100 mg/1
Pharmacologic classes
Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
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
27437-203-11EA - Each27437-203403be90a-8117-4a6d-98f6-11435eea63d212013-02-13

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
27437-203-02274370203021 BLISTER PACK in 1 CARTON (27437-203-02) > 1 TABLET, CHEWABLE in 1 BLISTER PACK1 blister pack2012-12-050000-00-00NoNoCurrent
27437-203-082743702030850 TABLET, CHEWABLE in 1 BOTTLE (27437-203-08) 2012-12-050000-00-00NoNoCurrent
27437-203-102743702031010 TABLET, CHEWABLE in 1 BOTTLE (27437-203-10) 2012-12-050000-00-00NoNoCurrent
27437-203-11274370203111 BLISTER PACK in 1 CARTON (27437-203-11) > 10 TABLET, CHEWABLE in 1 BLISTER PACK1 blister pack2012-12-050000-00-00NoNoCurrent