Amoxicillin and Clavulanate Potassium

Product NDC
68071-2431
11-digit product format
680712431
Labeler code
68071
Product ID
68071-2431_c3bb33ce-8aaa-5156-e053-2a95a90ac4a7
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amoxicillin and Clavulanate Potassium
Dosage form
TABLET
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
NDA050720
Marketing category
NDA
Marketing start
2019-12-12
Marketing end
0000-00-00
Substance
AMOXICILLIN; CLAVULANATE POTASSIUM
Active strength
875 mg/1; mg/1
Pharmacologic classes
Penicillin-class Antibacterial [EPC],Penicillins [CS],beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68071-2431-16807124310110 TABLET in 1 BOTTLE (68071-2431-1) 10 tablet2021-06-010000-00-00NoNoCurrent
68071-2431-36807124310330 TABLET in 1 BOTTLE (68071-2431-3) 30 tablet2021-06-010000-00-00NoNoCurrent
68071-2431-46807124310414 TABLET in 1 BOTTLE (68071-2431-4) 14 tablet2021-06-010000-00-00NoNoCurrent
68071-2431-56807124310515 TABLET in 1 BOTTLE (68071-2431-5) 15 tablet2021-06-010000-00-00NoNoCurrent