Primaquine Phosphate
- Product NDC
- 43063-225
- 11-digit product format
- 430630225
- Labeler code
- 43063
- Product ID
- 43063-225_db70b191-9771-789e-e053-2995a90a1b0c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Primaquine Phosphate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- NDA008316
- Marketing category
- NDA
- Marketing start
- 2011-04-15
- Marketing end
- 0000-00-00
- Substance
- PRIMAQUINE PHOSPHATE
- Active strength
- 15 mg/1
- Pharmacologic classes
- Antimalarial [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43063-225-14 | 43063022514 | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-225-14) | 2011-04-22 | 0000-00-00 | No | No | Current |
| 43063-225-28 | 43063022528 | 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-225-28) | 2011-04-22 | 0000-00-00 | No | No | Current |