Hydroxychloroquine Sulfate
- Product NDC
- 67296-1780
- 11-digit product format
- 672961780
- Labeler code
- 67296
- Product ID
- 67296-1780_d61f5644-21dc-08db-e053-2995a90aaa31
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxychloroquine Sulfate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA040104
- Marketing category
- ANDA
- 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 |
|---|
| 67296-1780-1 | Hydroxychloroquine Sulfate | 12 in 1 BOTTLE | TABLET, FILM COATED | 12 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1780 | HYDROXYCHLOROQUINE SULFATE TABLET, FILM COATED [REDPHARM DRUG, INC.] | 3 | Legacy NDC, 1 package rows | 20220123_a3c2b92b-1bb7-d83c-e053-2a95a90a8fc2.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 |
|---|
| 67296-1780-1 | 67296178001 | 12 TABLET, FILM COATED in 1 BOTTLE (67296-1780-1) | 2020-01-01 | 0000-00-00 | No | No | Current |