NDC product
Simethicone 125 mg
NDC 17856-0137 · ATLANTIC BIOLOGICALS CORP.
Key facts
| Product NDC | 17856-0137 |
|---|---|
| Proprietary name | Simethicone 125 mg |
| Nonproprietary name | Simethicone |
| Substances | DIMETHICONE |
| Dosage form | TABLET, CHEWABLE |
| Route | ORAL |
| Labeler | ATLANTIC BIOLOGICALS CORP. |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M002 |
| Pharmacologic classes | Skin Barrier Activity [PE] |
| Marketing start | Apr 25, 2018 |
| 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: