Raloxifene Hydrochloride
- Product NDC
- 63629-7708
- 11-digit product format
- 636297708
- Labeler code
- 63629
- Product ID
- 63629-7708_29a280c3-008f-440b-9fa4-0f514342e3bd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Raloxifene
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090842
- Marketing category
- ANDA
- Marketing start
- 2016-06-29
- 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
- 2021-12-31
- 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 |
|---|
| 63629-7708-1 | 63629770801 | 30 TABLET in 1 BOTTLE (63629-7708-1) | 30 tablet | 2018-07-02 | 0000-00-00 | No | No | Current |
| 63629-7708-2 | 63629770802 | 60 TABLET in 1 BOTTLE (63629-7708-2) | 60 tablet | 2018-07-02 | 0000-00-00 | No | No | Current |
| 63629-7708-3 | 63629770803 | 90 TABLET in 1 BOTTLE (63629-7708-3) | 90 tablet | 2018-07-02 | 0000-00-00 | No | No | Current |
| 63629-7708-4 | 63629770804 | 300 TABLET in 1 BOTTLE (63629-7708-4) | 300 tablet | 2018-07-02 | 0000-00-00 | No | No | Current |
| 63629-7708-5 | 63629770805 | 500 TABLET in 1 BOTTLE (63629-7708-5) | 500 tablet | 2018-07-02 | 0000-00-00 | No | No | Current |