NDC codes

FDA NDC Directory
Product NDC (as listed)49035-703Labeler and product segments. Claims need a package NDC.
Product NDC at billing width49035-0703Add 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
49035-703-01490350703011 BOTTLE, SPRAY in 1 BOTTLE, SPRAY (49035-703-01) / 120 SPRAY, METERED in 1 BOTTLE, SPRAYMarketed from Jul 1, 2025

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)
Budesonide
Generic name (nonproprietary)
budesonide
Active ingredients
Budesonide32 ug/1
Dosage form
Spray, Metered
Route
Nasal
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078949
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 49035-703_fce82ec5-1379-4faa-a710-f989c6c9ca5aSPL ID fce82ec5-1379-4faa-a710-f989c6c9ca5aSPL set ID d9ba3859-90af-0390-11be-c04834e27d61RxCUI 1797929UNII Q3OKS62Q6X
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 HCPCS code in Med-Code's directory. Nasal products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N449035070301 followed by a unit qualifier and the quantity

Package 49035-0703-01. 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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Use s Temporarily relieves these symptoms of hay fever or other upper respiratory allergies: • nasal congestion • runny nose • itchy nose • sneezing

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 078949

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

FDA NDC Directory listings under ANDA 078949
ProductStrengthForm · routeLabelerProduct NDC
BudesonideBudesonide 32 ug/1Spray, MeteredNasalRugby Laboratories0536-1112
BudesonideBudesonide 32 ug/1Spray, MeteredNasalCVS Pharmacy69842-001
BudesonideBudesonide 32 ug/1Spray, MeteredNasalWalgreens0363-0048
BudesonideBudesonide 32 ug/1Spray, MeteredNasalRugby Laboratories0536-1456
BudesonideBudesonide 32 ug/1Spray, MeteredNasalApotex Corp.60505-6129

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