NDC product
LIQUID · Allergan, Inc.
NDC 0023-1111 · Allergan, Inc.
Key facts
| Product NDC | 0023-1111 |
|---|---|
| Nonproprietary name | botulinum toxin type A |
| Substances | BOTULINUM TOXIN TYPE A |
| Dosage form | LIQUID |
| Labeler | Allergan, Inc. |
| Product type | BULK INGREDIENT |
| Marketing category | BULK INGREDIENT |
| Marketing start | Dec 15, 1989 |
| 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: