NDC product
Humco Sodium Bicarbonate
NDC 0395-2685 · Humco Holding Group, Inc.
Key facts
| Product NDC | 0395-2685 |
|---|---|
| Proprietary name | Humco Sodium Bicarbonate |
| Nonproprietary name | Sodium Bicarbonate |
| Substances | SODIUM BICARBONATE |
| Dosage form | POWDER |
| Route | ORAL |
| Labeler | Humco Holding Group, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M001 |
| Pharmacologic classes | Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC] |
| Marketing start | Mar 25, 1998 |
| Listing certified through | Dec 31, 2027 |
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: