Hydroxychloroquine Sulfate
- Product NDC
- 16714-753
- 11-digit product format
- 167140753
- Labeler code
- 16714
- Product ID
- 16714-753_093d7e63-6755-4408-8856-7b8c22792de2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxychloroquine Sulfate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Northstar RxLLC
- Application
- ANDA040104
- Marketing category
- ANDA
- Marketing start
- 2019-08-01
- Marketing end
- 2022-10-31
- 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 |
|---|
| 16714-753-01 | 16714075301 | 100 TABLET, FILM COATED in 1 BOTTLE (16714-753-01) | 2019-08-01 | 2022-10-31 | No | No | Current |