Plaquenil
- Product NDC
- 42291-335
- 11-digit product format
- 422910335
- Labeler code
- 42291
- Product ID
- 42291-335_834a7ea8-a22f-6797-e053-2a91aa0a260c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxychloroquine Sulfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE, Inc.
- Application
- NDA009768
- Marketing category
- NDA
- Marketing start
- 2016-07-14
- Marketing end
- 2019-03-31
- Substance
- HYDROXYCHLOROQU
- Active strength
- 200 mg/1
- Pharmacologic classes
- Antirheumatic A
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record