Amoxicillin

Product NDC
21695-544
11-digit product format
216950544
Labeler code
21695
Product ID
21695-544_ee3875c6-5c49-4386-8ad2-5fe3208ed9e9
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amoxicillin
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Rebel Distributors Corp.
Application
ANDA065228
Marketing category
ANDA
Marketing start
2005-07-13
Marketing end
0000-00-00
Substance
AMOXICILLIN
Active strength
875 mg/1
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
502415e5-4ac7-4266-a01a-ef44aa3c028dProduct name720250623
d0f377c9-74d8-e2e3-e06e-4d37534f5c0fProduct name320250620
2ebbc361-d28f-48a9-a286-c1ae09cdaf5cProduct name320230314
2bb254ff-3d7f-4bdb-abf9-476506008c55Product name120230117
f33561b9-47cb-411c-a228-16c62e346cd4Product name120200415
8690a824-4bf8-4d1e-b118-2d6dda86bc04Product name220161206
cf3f1c02-1f32-2322-3314-b70ebbf5610eProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
21695-544-202019-09-24C16284748780-1934fe258-4962-48b1-e053-8cdaa90a720aAmoxicillin Capsules, Tablets and Powder for Oral Suspension, USP

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
21695-544-20EA - Each21695-544a46a17e5-2a5a-4b30-9057-4934c3e66b5212012-07-24

DailyMed Socrata Ingredients#