Hydroxychloroquine Sulfate
- Product NDC
- 42292-011
- 11-digit product format
- 422920011
- Labeler code
- 42292
- Product ID
- 42292-011_7cef9597-5932-339f-e053-2991aa0a1efb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxychloroquine Sulfate
- Dosage form
- TABLET, FILM COATED
- Route
- ENTERAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA040274
- Marketing category
- ANDA
- Marketing start
- 2016-03-28
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42292-011-06 | 42292001106 | 50 BLISTER PACK in 1 CARTON (42292-011-06) > 1 TABLET, FILM COATED in 1 BLISTER PACK (42292-011-01) | 50 blister pack | 2016-03-28 | 0000-00-00 | No | No | Current |