ACTONEL

Product NDC
0149-0470
11-digit product format
001490470
Labeler code
0149
Product ID
0149-0470_05985725-417c-44f4-9e38-4fed7cdfdaad
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
RISEDRONATE SODIUM
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Warner Chilcott Pharmaceuticals Inc.
Application
NDA020835
Marketing category
NDA
Marketing start
1998-03-27
Marketing end
0000-00-00
Substance
RISEDRONATE SODIUM
Active strength
30 mg/1
Pharmacologic classes
Bisphosphonate [EPC],Diphosphonates [CS]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0149-0470-012021-01-07C16284748780-1956f9ecf-bf97-621f-e053-dbdaa90a74ad563c6d6d-56df-43a7-a7aa-709c5ea3cdbe
0149-0470-012019-10-21C16284748780-1956f9ecf-bf97-621f-e053-dbdaa90a74ad563c6d6d-56df-43a7-a7aa-709c5ea3cdbe