ACD Solution Modified
- Product NDC
- 51808-201
- 11-digit product format
- 518080201
- Labeler code
- 51808
- Product ID
- 51808-201_651af678-d1d2-4e8e-8fe0-ae6c0ba11a16
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ACD Solution Modified
- Dosage form
- SOLUTION
- Route
- INTRAVENOUS
- Labeler
- AnazaoHealth Corporation
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2012-05-23
- Marketing end
- 0000-00-00
- Substance
- ANHYDROUS CITRIC ACID
- Active strength
- 8 mg/mL
- Pharmacologic classes
- Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51808-201-01 | ACD Solution Modified | 10 mL in 1 VIAL | SOLUTION | 10 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51808-201 | ACD SOLUTION MODIFIED SOLUTION [ANAZAOHEALTH CORPORATION] | 1 | Legacy NDC, 1 package rows | 20120705_64a9b51b-c982-4d50-ab58-a5b9029a7602.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 51808-201-01 | 51808020101 | 10 mL in 1 VIAL | 10 ml | Historical |