NDC 71335-0897-09 - 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
- 71335-0897
- Requested NDC
- 71335-0897-09
- Package NDCs from labels
- 71335-0897-1, 71335-0897-2, 71335-0897-3, 71335-0897-4, 71335-0897-5, 71335-0897-6, 71335-0897-7, 71335-0897-8, 71335-0897-9, 71335-0897-09
- Manufacturer
- Bryant Ranch Prepack
- Effective date
- 2024-07-09
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Hydroxychloroquine sulfate - Bryant Ranch Prepack | Bryant Ranch Prepack | 2024-07-09 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71335-0897-1 | Hydroxychloroquine sulfate | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | 9 | |
| 71335-0897-2 | Hydroxychloroquine sulfate | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | 9 | |
| 71335-0897-3 | Hydroxychloroquine sulfate | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | 9 | |
| 71335-0897-4 | Hydroxychloroquine sulfate | 180 in 1 BOTTLE | TABLET, FILM COATED | 180 | 9 | |
| 71335-0897-5 | Hydroxychloroquine sulfate | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | 9 | |
| 71335-0897-6 | Hydroxychloroquine sulfate | 120 in 1 BOTTLE | TABLET, FILM COATED | 120 | 9 | |
| 71335-0897-7 | Hydroxychloroquine sulfate | 10 in 1 BOTTLE | TABLET, FILM COATED | 10 | 9 | |
| 71335-0897-8 | Hydroxychloroquine sulfate | 14 in 1 BOTTLE | TABLET, FILM COATED | 14 | 9 | |
| 71335-0897-9 | Hydroxychloroquine sulfate | 20 in 1 BOTTLE | TABLET, FILM COATED | 20 | 9 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 71335-0897 | HYDROXYCHLOROQUINE SULFATE TABLET, FILM COATED [BRYANT RANCH PREPACK] | 9 | Current NDC, Legacy NDC, 9 package rows | 20240724_f618a091-ade1-4c39-ab76-f6218b606e05.zip |
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.