Hydroxychloroquine Sulfate
- Product NDC
- 76385-144
- 11-digit product format
- 763850144
- Labeler code
- 76385
- Product ID
- 76385-144_f07d0fea-0943-7af4-e053-2995a90a95c9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxychloroquine Sulfate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bayshore Pharmaceuticals LLC
- Application
- ANDA040766
- Marketing category
- ANDA
- Marketing start
- 2020-05-08
- Marketing end
- 0000-00-00
- Substance
- HYDROXYCHLOROQUINE SULFATE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Antimalarial [EPC], Antirheumatic Agent [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 76385-144-01 | 76385014401 | 100 TABLET, FILM COATED in 1 BOTTLE (76385-144-01) | 2020-05-08 | 0000-00-00 | No | No | Current |
| 76385-144-50 | 76385014450 | 500 TABLET, FILM COATED in 1 BOTTLE (76385-144-50) | 2020-05-08 | 0000-00-00 | No | No | Current |