Hydroxychloroquine Sulfate
- Product NDC
- 0615-8374
- 11-digit product format
- 006158374
- Labeler code
- 0615
- Product ID
- 0615-8374_e6715b5f-79f1-4537-852d-88779452b26b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxychloroquine Sulfate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA040081
- Marketing category
- ANDA
- Marketing start
- 2020-10-08
- Marketing end
- 2022-09-30
- 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 |
|---|
| 0615-8374-39 | 00615837439 | 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8374-39) | 2020-12-11 | 0000-00-00 | No | No | Current |