HYDROXYCHLOROQUINE SULFATE
- Product NDC
- 0378-0373
- 11-digit product format
- 003780373
- Labeler code
- 0378
- Product ID
- 0378-0373_51167105-95c4-402e-97a4-df909931d7ec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HYDROXYCHLOROQUINE SULFATE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Mylan Pharmaceuticals Inc.
- Application
- ANDA040274
- Marketing category
- ANDA
- Marketing start
- 1998-06-18
- Marketing end
- 2023-04-30
- Substance
- HYDROXYCHLOROQUINE SULFATE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Antimalarial [EPC], Antirheumatic Agent [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 |
|---|
| 0378-0373-01 | 00378037301 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0373-01) | 1998-06-18 | 2023-04-30 | No | No | Current |