NDC codes

FDA NDC Directory
Product NDC (as listed)13107-231Labeler and product segments. Claims need a package NDC.
Product NDC at billing width13107-0231Add 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 NDC11-digit (billing)PackageCopy
13107-231-54131070231541 CANISTER in 1 CARTON (13107-231-54) / 120 AEROSOL, METERED in 1 CANISTERMarketed from Sep 14, 2026

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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)
Beclomethasone Dipropionate
Generic name (nonproprietary)
beclomethasone dipropionate
Active ingredients
Beclomethasone dipropionate — 80 ug/1
Dosage form
Aerosol, Metered
Route
Respiratory (Inhalation)
Labeler
Aurolife Pharma LLCNDC labeler code 13107
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 214418
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 13107-231_a27795ec-4309-4a40-8dc2-12d0ec5bf12bSPL ID a27795ec-4309-4a40-8dc2-12d0ec5bf12b
Pharmacologic class
Corticosteroid

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.

NDC on a medical claim

N413107023154 followed by a unit qualifier and the quantity

Package 13107-0231-54. 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 13107-231

What is NDC 13107-231?
13107-231 is the product NDC for Beclomethasone Dipropionate, Beclomethasone dipropionate 80 ug/1 aerosol, metered, listed with the FDA by Aurolife Pharma LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Beclomethasone Dipropionate.
What is the active ingredient?
Beclomethasone dipropionate.
Who is the labeler?
Aurolife Pharma LLC, NDC labeler code 13107. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Beclomethasone Dipropionate?
3 other product NDCs are listed under this name. See all Beclomethasone Dipropionate NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Beclomethasone Dipropionate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Beclomethasone DipropionateBeclomethasone dipropionate 40 ug/1Aerosol, MeteredRespiratory (Inhalation)Aurolife Pharma LLC13107-23013107-0230-54
Beclomethasone DipropionateBeclomethasone dipropionate 40 ug/1Aerosol, MeteredRespiratory (Inhalation)Amneal Pharmaceuticals NY LLC69238-128969238-1289-04
Beclomethasone DipropionateBeclomethasone dipropionate 80 ug/1Aerosol, MeteredRespiratory (Inhalation)Amneal Pharmaceuticals NY LLC69238-129069238-1290-04

Other NDCs under ANDA 214418

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

FDA NDC Directory listings under ANDA 214418
ProductStrengthForm · routeLabelerProduct NDC
Beclomethasone DipropionateBeclomethasone dipropionate 40 ug/1Aerosol, MeteredRespiratory (Inhalation)Aurolife Pharma LLC13107-230

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Beclomethasone Dipropionate NDC 13107-231 | Med-Code