Hydroxychloroquine Sulfate
- Product NDC
- 68788-7770
- 11-digit product format
- 687887770
- Labeler code
- 68788
- Product ID
- 68788-7770_35e525e4-5a35-40a1-a192-c52377bf8591
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxychloroquine Sulfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- NDA009768
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2020-08-03
- Marketing end
- 0000-00-00
- Substance
- HYDROXYCHLOROQUINE SULFATE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Antirheumatic Agent [EPC],Antimalarial [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7770-1 | 68788777001 | 100 TABLET in 1 BOTTLE (68788-7770-1) | 100 tablet | 2020-08-03 | 0000-00-00 | No | No | Current |
| 68788-7770-2 | 68788777002 | 20 TABLET in 1 BOTTLE (68788-7770-2) | 20 tablet | 2020-08-03 | 0000-00-00 | No | No | Current |
| 68788-7770-3 | 68788777003 | 30 TABLET in 1 BOTTLE (68788-7770-3) | 30 tablet | 2020-08-03 | 0000-00-00 | No | No | Current |
| 68788-7770-4 | 68788777004 | 24 TABLET in 1 BOTTLE (68788-7770-4) | 24 tablet | 2020-08-03 | 0000-00-00 | No | No | Current |
| 68788-7770-8 | 68788777008 | 8 TABLET in 1 BOTTLE (68788-7770-8) | 8 tablet | 2020-08-03 | 0000-00-00 | No | No | Current |