Cephalexin

Product NDC
71205-591
11-digit product format
712050591
Labeler code
71205
Product ID
71205-591_ada7b8a5-98f4-454c-b38f-92192d4db33f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Cephalexin
Dosage form
CAPSULE
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA062702
Marketing category
ANDA
Marketing start
1990-09-30
Substance
CEPHALEXIN
Active strength
500 mg/1
Pharmacologic classes
Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
OBN7UDS42YCEPHALEXIN23325-78-2CEPHALEXIN

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71205-591-06712050591066 CAPSULE in 1 BOTTLE (71205-591-06) 6 capsule2021-08-06NoNoHistorical
71205-591-147120505911414 CAPSULE in 1 BOTTLE (71205-591-14) 14 capsule2021-08-06NoNoHistorical
71205-591-157120505911515 CAPSULE in 1 BOTTLE (71205-591-15) 15 capsule2021-08-06NoNoHistorical
71205-591-207120505912020 CAPSULE in 1 BOTTLE (71205-591-20) 20 capsule2021-08-06NoNoHistorical
71205-591-217120505912121 CAPSULE in 1 BOTTLE (71205-591-21) 21 capsule2021-08-06NoNoHistorical
71205-591-287120505912828 CAPSULE in 1 BOTTLE (71205-591-28) 28 capsule2021-08-06NoNoHistorical
71205-591-307120505913030 CAPSULE in 1 BOTTLE (71205-591-30) 30 capsule2021-08-06NoNoHistorical
71205-591-407120505914040 CAPSULE in 1 BOTTLE (71205-591-40) 40 capsule2021-08-06NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
CephalexinProficient Rx LP2021-08-01HUMAN PRESCRIPTION DRUG LABEL1