Hydroxychloroquine sulfate
- Product NDC
- 68071-2912
- 11-digit product format
- 680712912
- Labeler code
- 68071
- Product ID
- 68071-2912_f20028aa-cf0b-a30a-e053-2a95a90a8c98
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxychloroquine sulfate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA040657
- Marketing category
- ANDA
- Marketing start
- 2008-01-03
- 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
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-2912-2 | Hydroxychloroquine sulfate | 12 in 1 BOTTLE | TABLET, FILM COATED | 12 | | 4 |
| 68071-2912-3 | Hydroxychloroquine sulfate | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 4 |
| 68071-2912-9 | Hydroxychloroquine sulfate | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2912 | HYDROXYCHLOROQUINE SULFATE TABLET, FILM COATED [NUCARE PHARMACEUTICALS,INC.] | 4 | Legacy NDC, 3 package rows | 20231121_f2002851-852f-4ee8-e053-2a95a90a242d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2912-2 | 68071291202 | 12 in 1 BOTTLE | | | | | Historical |
| 68071-2912-3 | 68071291203 | 30 in 1 BOTTLE | | | | | Historical |
| 68071-2912-9 | 68071291209 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-2912-9) | 2023-01-11 | 0000-00-00 | No | No | Current |