NDC product
Nicotine Mini
NDC 0536-1239 · Rugby Laboratories, Inc.
Key facts
| Product NDC | 0536-1239 |
|---|---|
| Proprietary name | Nicotine Mini |
| Nonproprietary name | nicotine polacrilex |
| Substances | NICOTINE |
| Dosage form | LOZENGE |
| Route | ORAL |
| Labeler | Rugby Laboratories, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | ANDA |
| Application number | ANDA207868 |
| Pharmacologic classes | Cholinergic Nicotinic Agonist [EPC], Nicotine [CS] |
| Marketing start | Jul 31, 2019 |
| 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: