NDC product
Standardized Redtop Pollen
NDC 22840-0207 · Greer Laboratories, Inc.
Key facts
| Product NDC | 22840-0207 |
|---|---|
| Proprietary name | Standardized Redtop Pollen |
| Nonproprietary name | Agrostis alba |
| Substances | AGROSTIS GIGANTEA POLLEN |
| Dosage form | SOLUTION |
| Route | INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS |
| Labeler | Greer Laboratories, Inc. |
| Product type | STANDARDIZED ALLERGENIC |
| Marketing category | BLA |
| Application number | BLA101840 |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Pollen Allergenic Extract [EPC], Pollen [CS] and 1 more |
| Marketing start | Sep 15, 1968 |
| 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: