LeukoTrap SOLX A Additive
- Product NDC
- 53157-002
- 11-digit product format
- 531570002
- Labeler code
- 53157
- Product ID
- 53157-002_eab5a1f9-bed2-4a42-9544-d5912cd267b8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AS-7 A Additive Solution
- Dosage form
- SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Haemonetics Manufacturing Inc
- Application
- NDA110059
- Marketing category
- NDA
- Marketing start
- 2015-11-12
- Marketing end
- 0000-00-00
- Substance
- ADENINE; MANNITOL
- Active strength
- 0 g/80mL; g/80mL
- Pharmacologic classes
- Increased Diuresis [PE],Osmotic Activity [MoA],Osmotic Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#