Hydroxychloroquine Sulfate
- Product NDC
- 66993-057
- 11-digit product format
- 669930057
- Labeler code
- 66993
- Product ID
- 66993-057_f72a17f3-b730-4988-893f-e49b949c7a0f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxychloroquine Sulfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Prasco Laboratories
- Application
- NDA009768
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2014-12-12
- Marketing end
- 2022-10-31
- Substance
- HYDROXYCHLOROQUINE SULFATE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Antirheumatic Agent [EPC],Antimalarial [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 66993-057-02 | 66993005702 | 100 TABLET in 1 BOTTLE (66993-057-02) | 100 tablet | 2014-12-12 | 0000-00-00 | No | No | Current |
| 66993-057-04 | 66993005704 | 500 TABLET in 1 BOTTLE (66993-057-04) | 500 tablet | 2015-06-10 | 0000-00-00 | No | No | Current |