Amoxicillin and Clavulanate Potassium

Product NDC
68788-9043
11-digit product format
687889043
Labeler code
68788
Product ID
68788-9043_0bed6588-89b6-4536-bc92-fed4bc7bcbdb
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amoxicillin and Clavulanate Potassium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Preferred Pharmaceuticals, Inc.
Application
ANDA065096
Marketing category
ANDA
Marketing start
2012-01-25
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
68788-9043-2EA - Each68788-90434cb7f42c-56d1-4d2a-acb1-1d576817954d12015-02-02