Raloxifene Hydrochloride
- Product NDC
- 50090-3866
- 11-digit product format
- 500903866
- Labeler code
- 50090
- Product ID
- 50090-3866_833c033b-6909-427a-8dc2-230f31a554f1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Raloxifene Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA208206
- Marketing category
- ANDA
- Marketing start
- 2016-01-20
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-3866-0 | 50090386600 | 100 TABLET, FILM COATED in 1 BOTTLE (50090-3866-0) | 2018-11-27 | 0000-00-00 | No | No | Current |
| 50090-3866-1 | 50090386601 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3866-1) | 2016-01-20 | 0000-00-00 | No | No | Current |