Plaquenil
- Product NDC
- 67296-1781
- 11-digit product format
- 672961781
- Labeler code
- 67296
- Product ID
- 67296-1781_d61cc7c2-88c9-400d-e053-2a95a90ad7e7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxychloroquine Sulfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- NDA009768
- Marketing category
- NDA
- Marketing start
- 2020-01-01
- 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
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 |
|---|
| 67296-1781-1 | Plaquenil | 12 in 1 BOTTLE | TABLET | 12 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1781 | PLAQUENIL (HYDROXYCHLOROQUINE SULFATE) TABLET [REDPHARM DRUG, INC.] | 2 | Legacy NDC, 1 package rows | 20220123_a3c311ff-2f87-7780-e053-2995a90aac4e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67296-1781-1 | 67296178101 | 12 TABLET in 1 BOTTLE (67296-1781-1) | 12 tablet | 2020-01-01 | 0000-00-00 | No | No | Current |