NDC codes

FDA NDC Directory
Product NDC (as listed)70518-3560Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-3560Add 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
70518-3560-1705183560015 POUCH in 1 CARTON (70518-3560-1) / 5 VIAL in 1 POUCH / 3 mL in 1 VIALMarketed from Oct 19, 2022

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)
Albuterol Sulfate
Generic name (nonproprietary)
albuterol sulfate
Active ingredients
Albuterol sulfate — .83 mg/mL
Dosage form
Solution
Route
Respiratory (Inhalation)
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 207857
Marketing start
Listing expires
Other FDA classes
Adrenergic beta2-Agonists (Mechanism)
Identifiers
Product ID 70518-3560_54789a34-7ed6-8902-e063-6294a90a5b04SPL ID 54789a34-7ed6-8902-e063-6294a90a5b04SPL set ID 0f9bf2c8-55c0-4b4d-97de-d6c7220c3862RxCUI 630208UNII 021SEF3731
Pharmacologic class
beta2-Adrenergic Agonist

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

N470518356001 followed by a unit qualifier and the quantity

Package 70518-3560-01. 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)

INDICATIONS AND USAGE Albuterol inhalation solution is indicated for the relief of bronchospasm in patients 2 years of age and older with reversible obstructive airway disease and acute attacks of bronchospasm.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 207857

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

FDA NDC Directory listings under ANDA 207857
ProductStrengthForm · routeLabelerProduct NDC
Albuterol SulfateAlbuterol sulfate .83 mg/mLSolutionRespiratory (Inhalation)Preferred Pharmaceuticals Inc.68788-8492
Albuterol SulfateAlbuterol sulfate .83 mg/mLSolutionRespiratory (Inhalation)Proficient Rx LP71205-641
Albuterol SulfateAlbuterol sulfate .83 mg/mLSolutionRespiratory (Inhalation)Sun Pharmaceutical Industries, Inc.47335-703

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free Med-Code account to keep looking up NDCs, J-codes and drugs.

Create a free accountLog in