Amoxicillan

Product NDC
51655-157
11-digit product format
516550157
Labeler code
51655
Product ID
51655-157_7a891dd1-ed56-4f00-89fb-2d6be99252c9
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amoxicillan
Dosage form
CAPSULE
Route
ORAL
Labeler
Northwind Pharmaceuticals
Application
ANDA062881
Marketing category
ANDA
Marketing start
2014-06-01
Marketing end
0000-00-00
Substance
AMOXICILLIN
Active strength
500 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
51655-157-212024-02-23C16284748780-19d75b9d0-cad5-f424-e053-dadaa90a57ceda5e53f5-ac3c-43ab-9b05-dcfe6012dc2c
51655-157-212020-01-31C16284748780-19d75b9d0-cad5-f424-e053-dadaa90a57ceda5e53f5-ac3c-43ab-9b05-dcfe6012dc2c