NDC 68382-096-30 - Hydroxychloroquine sulfate
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 68382-096
- Requested NDC
- 68382-096-30
- Package NDCs from labels
- 68382-096-01, 68382-096-05, 68382-096-30, 68382-096-77
- Manufacturer
- Preferred Pharmaceuticals, Inc.
- Effective date
- 2026-05-11
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Hydroxychloroquine sulfate - Preferred Pharmaceuticals, Inc. | Preferred Pharmaceuticals, Inc. | 2026-05-11 | HUMAN PRESCRIPTION DRUG LABEL |
| Hydroxychloroquine sulfate - McKesson Corporation dba SKY Packaging | Legacy Pharmaceutical Packaging, LLC | McKesson Corporation dba SKY Packaging | Legacy Pharmaceutical Packaging, LLC | 2024-12-26 | HUMAN PRESCRIPTION DRUG LABEL |
| Hydroxychloroquine sulfate - A-S Medication Solutions | A-S Medication Solutions | 2024-10-15 | HUMAN PRESCRIPTION DRUG LABEL |
| Hydroxychloroquine sulfate - A-S Medication Solutions | A-S Medication Solutions | 2024-10-15 | HUMAN PRESCRIPTION DRUG LABEL |
| Hydroxychloroquine Sulfate - American Health Packaging | American Health Packaging | 2024-08-01 | HUMAN PRESCRIPTION DRUG LABEL |
| Hydroxychloroquine sulfate - Bryant Ranch Prepack | Bryant Ranch Prepack | 2024-07-09 | HUMAN PRESCRIPTION DRUG LABEL |
| Hydroxychloroquine sulfate - NCS HealthCare of KY, LLC dba Vangard Labs | NCS HealthCare of KY, LLC dba Vangard Labs | 2024-06-21 | HUMAN PRESCRIPTION DRUG LABEL |
| HYDROXYCHLOROQUINE - Zydus Pharmaceuticals USA Inc. | Zydus Lifesciences Limited | Zydus Pharmaceuticals USA Inc. | Zydus Lifesciences Limited | 2023-12-19 | HUMAN PRESCRIPTION DRUG LABEL |
| Hydroxychloroquine sulfate - NuCare Pharmaceuticals,Inc. | NuCare Pharmaceuticals,Inc. | 2023-11-20 | HUMAN PRESCRIPTION DRUG LABEL |
| Hydroxychloroquine sulfate tablets, USP | NuCare Pharmaceuticals,Inc. | 2022-01-20 | HUMAN PRESCRIPTION DRUG LABEL |
| Hydroxychloroquine sulfate - Aphena Pharma Solutions - Tennessee, LLC | Aphena Pharma Solutions - Tennessee, LLC | 2020-12-22 | HUMAN PRESCRIPTION DRUG LABEL |
| HYDROXYCHLOROQUINE SULFATE - DIRECT RX | DIRECT RX | 2016-10-27 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68382-096-01 | Hydroxychloroquine sulfate | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | 11 | |
| 68382-096-05 | Hydroxychloroquine sulfate | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | 11 | |
| 68382-096-30 | Hydroxychloroquine sulfate | 1 in 1 BLISTER PACK | TABLET, FILM COATED | 1 | 11 | |
| 68382-096-77 | Hydroxychloroquine sulfate | 100 in 1 CARTON | TABLET, FILM COATED | 100 | 11 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 68382-096-01 | EA - Each | 68382-096 | 1ad94c26-4b39-4410-9089-964e237ae872 | 1 | 2012-07-24 |
| 68382-096-05 | EA - Each | 68382-096 | dd0cb769-0b6a-4de0-a1f3-d794b00a31a5 | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.