Raloxifene Hydrochloride
- Product NDC
- 70518-2994
- 11-digit product format
- 705182994
- Labeler code
- 70518
- Product ID
- 70518-2994_ba4bd825-6c23-00e4-e053-2995a90a2b4c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Raloxifene Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078193
- Marketing category
- ANDA
- Marketing start
- 2021-01-17
- Marketing end
- 0000-00-00
- Substance
- RALOXIFENE HYDROCHLORIDE
- Active strength
- 60 mg/1
- Pharmacologic classes
- Estrogen Agonist/Antagonist [EPC],Selective Estrogen Receptor Modulators [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2994-0 | 70518299400 | 30 POUCH in 1 BOX (70518-2994-0) > 1 TABLET, FILM COATED in 1 POUCH (70518-2994-1) | 30 pouch | 2021-01-17 | 0000-00-00 | No | No | Current |