What is NDC 22840-0301?

22840-0301 is the product NDC for Short and Giant Ragweed Pollen Mix, Ambrosia artemisiifolia pollen .025 g/mL; Ambrosia trifida pollen .025 g/mL solution, listed with the FDA by Greer Laboratories, Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Short and Giant Ragweed Pollen Mix (Ambrosia artemisiifolia and Ambrosia trifida).

What is the active ingredient?

Ambrosia artemisiifolia pollen, Ambrosia trifida pollen.

Greer Laboratories, Inc., NDC labeler code 22840. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Short and Giant Ragweed Pollen Mix?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Short and Giant Ragweed Pollen Mix NDC 22840-0301

NDC codes

FDA NDC Directory

Product NDC (as listed)22840-0301Labeler and product segments. Claims need a package NDC.

Product NDC at billing width22840-0301Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package
22840-0301-2	2284003010222840030102	10 mL in 1 VIAL, MULTI-DOSE (22840-0301-2)Marketed from Sep 15, 1981
22840-0301-4	2284003010422840030104	50 mL in 1 VIAL, MULTI-DOSE (22840-0301-4)Marketed from Sep 15, 1981
22840-0301-5	2284003010522840030105	5 mL in 1 BOTTLE, DROPPER (22840-0301-5)Marketed from Sep 15, 1981

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Short and Giant Ragweed Pollen Mix
Generic name (nonproprietary): ambrosia artemisiifolia and ambrosia trifida
Active ingredients: Ambrosia artemisiifolia pollen — .025 g/mLAmbrosia trifida pollen — .025 g/mL
Dosage form: Solution
Route: Intradermal, Percutaneous, Subcutaneous
Labeler: Greer Laboratories, Inc.NDC labeler code 22840
Product type: Non-standardized allergenic
Marketing category: BLA — Biologics License ApplicationApplication BLA 101844
Marketing start: Sep 15, 1981
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Pollen (Chemical structure)Pollen (Chemical structure)
Identifiers: Product ID 22840-0301_36ac5d19-78f4-b1f4-e063-6294a90ae4cbSPL ID 36ac5d19-78f4-b1f4-e063-6294a90ae4cb
Pharmacologic class: Non-Standardized Pollen Allergenic Extract; Standardized Pollen Allergenic Extract

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

Administration

Drug administration (CPT 96360–96549)

When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.

How CPT relates to drug billing

NDC on a medical claim

N422840030102 followed by a unit qualifier and the quantity

Package 22840-0301-02. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

The FDA listing for this product does not reference a label (SPL) set.

About NDC 22840-0301

What is NDC 22840-0301?: 22840-0301 is the product NDC for Short and Giant Ragweed Pollen Mix, Ambrosia artemisiifolia pollen .025 g/mL; Ambrosia trifida pollen .025 g/mL solution, listed with the FDA by Greer Laboratories, Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Short and Giant Ragweed Pollen Mix (Ambrosia artemisiifolia and Ambrosia trifida).
What is the active ingredient?: Ambrosia artemisiifolia pollen, Ambrosia trifida pollen.
Who is the labeler?: Greer Laboratories, Inc., NDC labeler code 22840. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Short and Giant Ragweed Pollen Mix?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other NDCs under BLA 101844

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under BLA 101844
Product	Strength	Form · route	Labeler	Product NDC
Short Ragweed Pollenambrosia artemisiifolia	Ambrosia artemisiifolia pollen .05 g/mL	SolutionIntradermal, Percutaneous, Subcutaneous	Greer Laboratories, Inc.	22840-0300