Amoxicillin

Product NDC
68788-8977
11-digit product format
687888977
Labeler code
68788
Product ID
68788-8977_85308e96-d3bc-47fd-b9b7-3988db75e605
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amoxicillin
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA065256
Marketing category
ANDA
Marketing start
2016-01-20
Marketing end
0000-00-00
Substance
AMOXICILLIN
Active strength
875 mg/1
Pharmacologic classes
Penicillin-class Antibacterial [EPC],Penicillins [CS]
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
68788-8977-22020-11-05C16284748780-19d75b9cf-e642-f424-e053-dadaa90a57ce9278e4f5-9c4a-407c-ba87-54682e9d247d
68788-8977-22020-01-31C16284748780-19d75b9cf-e642-f424-e053-dadaa90a57ce9278e4f5-9c4a-407c-ba87-54682e9d247d