NDC product
HEB Nicotine
NDC 37808-863 · H E B
Key facts
| Product NDC | 37808-863 |
|---|---|
| Proprietary name | HEB Nicotine |
| Nonproprietary name | nicotine polacrilex |
| Substances | NICOTINE |
| Dosage form | GUM, CHEWING |
| Route | ORAL |
| Labeler | H E B |
| Product type | HUMAN OTC DRUG |
| Marketing category | ANDA |
| Application number | ANDA206394 |
| Pharmacologic classes | Cholinergic Nicotinic Agonist [EPC], Nicotine [CS] |
| Marketing start | Jun 28, 2023 |
| 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: