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#