Amoxicillin

Product NDC
68788-9033
11-digit product format
687889033
Labeler code
68788
Product ID
68788-9033_11f5d0c7-4933-4d96-b974-ed1f985b9ae5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amoxicillin
Dosage form
CAPSULE
Route
ORAL
Labeler
Preferred Pharmaceuticals, Inc.
Application
ANDA065291
Marketing category
ANDA
Marketing start
2010-01-01
Marketing end
0000-00-00
Substance
AMOXICILLIN
Active strength
500 mg/1
Pharmacologic classes
Penicillin-class Antibacterial [EPC],Penicillins [CS]
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68788-9033-3EA - Each68788-903332f6c7b7-79bd-4850-9842-de6324337a9812015-02-02