ACD-A
- Product NDC
- 0942-9005
- 11-digit product format
- 009429005
- Labeler code
- 0942
- Product ID
- 0942-9005_26a93e4e-50c7-42d2-b169-c3ce9a89d106
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Antiocoagulant Citrate Dextrose Solution, Formula A
- Dosage form
- SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Fenwal, Inc.
- Application
- BN160918
- Marketing category
- NDA
- Marketing start
- 2012-10-24
- Marketing end
- 0000-00-00
- Substance
- ANHYDROUS CITRIC ACID; DEXTROSE MONOHYDRATE; SODIUM CITRATE, UNSPECIFIED FORM
- Active strength
- 730 mg/100mL; g/100mL; g/100mL
- Pharmacologic classes
- Acidifying Activity [MoA], Acidifying Activity [MoA], Anti-coagulant [EPC], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE], Decreased Coagulation Factor Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0942-9005 | ACD-A (ANTIOCOAGULANT CITRATE DEXTROSE SOLUTION, FORMULA A) SOLUTION [FENWAL, INC.] | 9 | Legacy NDC | 20221102_bee8e967-496c-4541-b092-ead6c8c80269.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0942-9005-01 | 00942900501 | 1000 mL in 1 BAG (0942-9005-01) | 1000 ml | 2012-10-24 | 0000-00-00 | No | No | Current |