Hydroxychloroquine Sulfate
- Product NDC
- 50090-5675
- 11-digit product format
- 500905675
- Labeler code
- 50090
- Product ID
- 50090-5675_d71a1388-7c38-4897-a178-b4a2e0931a87
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxychloroquine Sulfate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5675-1 | 50090567501 | 60 TABLET, FILM COATED in 1 BOTTLE (50090-5675-1) | 2021-09-20 | 0000-00-00 | No | No | Current |
| 50090-5675-2 | 50090567502 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-5675-2) | 2021-09-20 | 0000-00-00 | No | No | Current |