Hydroxychloroquine Sulfate
- Product NDC
- 43353-972
- 11-digit product format
- 433530972
- Labeler code
- 43353
- Product ID
- 43353-972_331bced4-a4ba-48d9-99fa-4a5c479529f2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxychloroquine Sulfate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA040766
- Marketing category
- ANDA
- Marketing start
- 2014-05-19
- Marketing end
- 0000-00-00
- Substance
- HYDROXYCHLOROQUINE SULFATE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Antirheumatic Agent [EPC],Antimalarial [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 43353-972-09 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-40b7-f424-e053-dadaa90a57ce | 192d7a55-a6f3-4e2a-ae46-5abc764e806f |
| 43353-972-53 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-40b7-f424-e053-dadaa90a57ce | 192d7a55-a6f3-4e2a-ae46-5abc764e806f |
| 43353-972-60 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-40b7-f424-e053-dadaa90a57ce | 192d7a55-a6f3-4e2a-ae46-5abc764e806f |
| 43353-972-80 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-40b7-f424-e053-dadaa90a57ce | 192d7a55-a6f3-4e2a-ae46-5abc764e806f |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 43353-972-09 | EA - Each | 43353-972 | 83d5441d-c527-4bf9-addb-3cfb410aad2f | 1 | 2016-07-19 |
| 43353-972-53 | EA - Each | 43353-972 | 183cc5e8-4e5d-41da-bcb7-b849c8e2baca | 1 | 2016-07-19 |
| 43353-972-60 | EA - Each | 43353-972 | 4ec74c98-5d07-4393-95b2-f126c1869f36 | 1 | 2016-07-19 |