Amoxicillin and Clavulanate Potassium

Product NDC
55700-106
11-digit product format
557000106
Labeler code
55700
Product ID
55700-106_8f00c4d1-31ee-4ddc-8ab1-1f91c4f5c3a1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amoxicillin and Clavulanate Potassium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
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
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55700-106-202021-02-03C16284748780-1ba0f9c33-0edd-a910-e053-dadaa90a0b856c6ac483-9efe-4df1-8a61-26dfda9a1182
55700-106-202021-01-29C16284748780-1ba0f9c33-0edd-a910-e053-dadaa90a0b856c6ac483-9efe-4df1-8a61-26dfda9a1182