Raloxifene Hydrochloride
- Product NDC
- 66993-661
- 11-digit product format
- 669930661
- Labeler code
- 66993
- Product ID
- 66993-661_d720873a-8c64-4be0-b47a-09ea0f076248
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Raloxifene Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Prasco Laboratories
- Application
- ANDA204310
- Marketing category
- ANDA
- Marketing start
- 2015-08-28
- Marketing end
- 2022-07-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 66993-661-02 | 66993066102 | 100 TABLET, FILM COATED in 1 BOTTLE (66993-661-02) | 2015-08-28 | 2022-07-31 | No | No | Current |
| 66993-661-30 | 66993066130 | 30 TABLET, FILM COATED in 1 BOTTLE (66993-661-30) | 2015-08-28 | 2022-07-31 | No | No | Current |
| 66993-661-88 | 66993066188 | 2000 TABLET, FILM COATED in 1 BOTTLE (66993-661-88) | 2015-08-28 | 2022-07-31 | No | No | Current |