Hydroxychloroquine Sulfate
- Product NDC
- 42385-927
- 11-digit product format
- 423850927
- Labeler code
- 42385
- Product ID
- 42385-927_04c03db9-7fbe-487e-ae70-551ce45088c8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxychloroquine Sulfate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Laurus Labs Limited
- Application
- ANDA210959
- Marketing category
- ANDA
- Marketing start
- 2019-09-05
- 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
- 2020-12-31
- 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 |
|---|
| 42385-927-01 | 42385092701 | 100 TABLET, FILM COATED in 1 BOTTLE (42385-927-01) | 2019-09-05 | 0000-00-00 | No | No | Current |
| 42385-927-05 | 42385092705 | 500 TABLET, FILM COATED in 1 BOTTLE (42385-927-05) | 2019-09-05 | 0000-00-00 | No | No | Current |