Hydroxychloroquine Sulfate
- Product NDC
- 0904-6884
- 11-digit product format
- 009046884
- Labeler code
- 0904
- Product ID
- 0904-6884_c1185262-baaa-4ab4-8915-3ea217a659a0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxychloroquine Sulfate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA040104
- Marketing category
- ANDA
- Marketing start
- 1995-11-30
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-6884-06 | 00904688406 | 50 BLISTER PACK in 1 CARTON (0904-6884-06) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 50 blister pack | 1995-11-30 | 0000-00-00 | No | No | Current |
| 0904-6884-61 | 00904688461 | 100 BLISTER PACK in 1 CARTON (0904-6884-61) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 100 blister pack | 1995-11-30 | 0000-00-00 | No | No | Current |