NDC product
Sodium Citrate and Citric Acid
NDC 0121-1190 · Pharmaceutical Associates, Inc.
Key facts
| Product NDC | 0121-1190 |
|---|---|
| Proprietary name | Sodium Citrate and Citric Acid |
| Nonproprietary name | SODIUM CITRATE and CITRIC ACID MONOHYDRATE |
| Substances | SODIUM CITRATE, ANHYDROUS CITRIC ACID |
| Dosage form | SOLUTION |
| Route | ORAL |
| Labeler | Pharmaceutical Associates, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Pharmacologic classes | Acidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE] |
| Marketing start | Jan 1, 1969 |
| Listing certified through | Dec 31, 2026 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: