Hydroxychloroquine Sulfate
- Product NDC
- 70954-172
- 11-digit product format
- 709540172
- Labeler code
- 70954
- Product ID
- 70954-172_9f450277-70b2-4721-88ec-df1bf3fe5262
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxychloroquine Sulfate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Novitium Pharma LLC
- Application
- NDA214581
- Marketing category
- NDA
- Marketing start
- 2022-01-14
- 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 |
|---|
| 70954-172-10 | 70954017210 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70954-172-10) | 2022-01-14 | 0000-00-00 | No | No | Current |
| 70954-172-20 | 70954017220 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70954-172-20) | 2022-01-14 | 0000-00-00 | No | No | Current |