Amoxicillin and Clavulanate Potassium

Product NDC
55700-456
11-digit product format
557000456
Labeler code
55700
Product ID
55700-456_cedcd1e2-6f0a-4ec9-bb21-d76c486c272d
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
ANDA065093
Marketing category
ANDA
Marketing start
2002-11-21
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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55700-456-14EA - Each55700-456c7fb5589-c8ee-45ef-984d-9b2e4317b1c912017-03-06