NDC product
A-30
NDC 58264-0322 · DNA Labs, Inc.
Key facts
| Product NDC | 58264-0322 |
|---|---|
| Proprietary name | A-30 |
| Nonproprietary name | TOBACCO LEAF |
| Substances | TOBACCO LEAF |
| Dosage form | SOLUTION |
| Route | SUBLINGUAL |
| Labeler | DNA Labs, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS] |
| Marketing start | Jan 1, 1990 |
| 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: