Hydroxychloroquine Sulfate
- Product NDC
- 0781-1407
- 11-digit product format
- 007811407
- Labeler code
- 0781
- Product ID
- 0781-1407_f6b15217-3b65-4d0e-8546-5056d71d525e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxychloroquine Sulfate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- ANDA040104
- Marketing category
- ANDA
- Marketing start
- 1995-11-30
- Marketing end
- 2021-12-31
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0781-1407-52 | 00781140752 | 500 TABLET, FILM COATED in 1 BOTTLE (0781-1407-52) | 2015-07-31 | 2021-09-30 | No | No | Current |
| 0781-1407-97 | 00781140797 | 100 TABLET, FILM COATED in 1 BOTTLE (0781-1407-97) | 2014-11-19 | 2021-12-31 | No | No | Current |