Amoxicillin and Clavulanate Potassium

Product NDC
68071-4032
11-digit product format
680714032
Labeler code
68071
Product ID
68071-4032_59410e9f-a584-7ee5-e053-2991aa0ac263
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amoxicillin and Clavulanate Potassium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA065096
Marketing category
ANDA
Marketing start
2002-10-31
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
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68071-4032-22020-05-22C16284748780-19d75b9d0-3487-f424-e053-dadaa90a57ce55f4b425-566b-6154-e054-00144ff8d46c
68071-4032-22020-01-31C16284748780-19d75b9d0-3487-f424-e053-dadaa90a57ce55f4b425-566b-6154-e054-00144ff8d46c

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68071-4032-2EA - Each68071-4032b53f525a-11ae-4d97-ae06-e8c95eb0853d12019-12-10