Cefdinir

Product NDC
71205-576
11-digit product format
712050576
Labeler code
71205
Product ID
71205-576_e9946b03-ade7-4c74-b94d-78c966bb0c89
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Cefdinir
Dosage form
CAPSULE
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA210220
Marketing category
ANDA
Marketing start
2021-02-20
Substance
CEFDINIR
Active strength
300 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
CI0FAO63WCCEFDINIR91832-40-5CEFDINIR

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71205-576-06712050576066 CAPSULE in 1 BOTTLE (71205-576-06) 6 capsule2021-07-23NoNoHistorical
71205-576-107120505761010 CAPSULE in 1 BOTTLE (71205-576-10) 10 capsule2021-07-23NoNoHistorical
71205-576-147120505761414 CAPSULE in 1 BOTTLE (71205-576-14) 14 capsule2021-07-23NoNoHistorical
71205-576-207120505762020 CAPSULE in 1 BOTTLE (71205-576-20) 20 capsule2021-07-23NoNoHistorical
71205-576-307120505763030 CAPSULE in 1 BOTTLE (71205-576-30) 30 capsule2021-07-23NoNoHistorical
71205-576-607120505766060 CAPSULE in 1 BOTTLE (71205-576-60) 60 capsule2021-07-23NoNoHistorical
71205-576-907120505769090 CAPSULE in 1 BOTTLE (71205-576-90) 90 capsule2021-07-23NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
CefdinirProficient Rx LP2022-05-01HUMAN PRESCRIPTION DRUG LABEL2