Amoxicillin

Product NDC
42708-011
11-digit product format
427080011
Labeler code
42708
Product ID
42708-011_3a2ba488-2d7a-4288-b49c-088777faed98
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amoxicillin
Dosage form
TABLET, COATED
Route
ORAL
Labeler
QPharma Inc
Application
ANDA065255
Marketing category
ANDA
Marketing start
2006-03-29
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
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
42708-011-202021-03-12C16284748780-1ba0f9c33-3df5-a910-e053-dadaa90a0b85ae355bbe-bbdc-43a0-aef3-1b52b960f3b0
42708-011-202021-01-29C16284748780-1ba0f9c33-3df5-a910-e053-dadaa90a0b85ae355bbe-bbdc-43a0-aef3-1b52b960f3b0