Hydroxychloroquine sulfate
- Product NDC
- 72789-026
- 11-digit product format
- 727890026
- Labeler code
- 72789
- Product ID
- 72789-026_db0bd082-e99f-4b04-e053-2995a90a17e8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxychloroquine sulfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA201691
- Marketing category
- ANDA
- Marketing start
- 2018-06-18
- Marketing end
- 0000-00-00
- Substance
- HYDROXYCHLOROQUINE SULFATE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Antimalarial [EPC], Antirheumatic Agent [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 72789-026-01 | 72789002601 | 100 TABLET in 1 BOTTLE, PLASTIC (72789-026-01) | 100 tablet | 2019-12-04 | 0000-00-00 | No | No | Current |