NDC product
injoy heartburn relief
NDC 0113-6023 · L. Perrigo Company
Key facts
| Product NDC | 0113-6023 |
|---|---|
| Proprietary name | injoy heartburn relief |
| Nonproprietary name | famotidine, calcium carbonate and magnesium hydroxide |
| Substances | FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE |
| Dosage form | TABLET, CHEWABLE |
| Route | ORAL |
| Labeler | L. Perrigo Company |
| Product type | HUMAN OTC DRUG |
| Marketing category | ANDA |
| Application number | ANDA077355 |
| Pharmacologic classes | Calculi Dissolution Agent [EPC], Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE] and 4 more |
| Marketing start | Aug 9, 2022 |
| 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: