What is NDC 68084-949?

68084-949 is the product NDC for Albuterol Sulfate, Albuterol sulfate 2 mg/1 tablet, listed with the FDA by American Health Packaging. It has 1 package NDC, shown above in 10- and 11-digit form.

American Health Packaging, NDC labeler code 68084. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Albuterol Sulfate?

89 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Albuterol Sulfate NDC 68084-949 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68084-949Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68084-0949Add 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	Copy
68084-949-25	68084094925	30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-949-25) / 1 TABLET in 1 BLISTER PACK (68084-949-95)Marketed from Sep 22, 2015

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): Albuterol Sulfate
Generic name (nonproprietary): albuterol sulfate
Active ingredients: Albuterol sulfate — 2 mg/1
Dosage form: Tablet
Route: Oral
Labeler: American Health PackagingNDC labeler code 68084
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 072637
Marketing start: Sep 22, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic beta2-Agonists (Mechanism)
Identifiers: Product ID 68084-949_1e7d3421-f562-17f5-e063-6294a90a9358SPL ID 1e7d3421-f562-17f5-e063-6294a90a9358SPL set ID b0f73459-baeb-42a7-be48-2c3647d9b205RxCUI 197316, 197318UNII 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 HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N468084094925 followed by a unit qualifier and the quantity

Package 68084-0949-25. 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 Jul 30, 2024.

Indications (excerpt from the label)

INDICATIONS AND USAGE Albuterol tablets are indicated for the relief of bronchospasm in adults and children 6 years of age and older with reversible obstructive airway disease.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68084-949

What is NDC 68084-949?: 68084-949 is the product NDC for Albuterol Sulfate, Albuterol sulfate 2 mg/1 tablet, listed with the FDA by American Health Packaging. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Albuterol Sulfate.
What is the active ingredient?: Albuterol sulfate.
Who is the labeler?: American Health Packaging, NDC labeler code 68084. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Albuterol Sulfate?: 89 other product NDCs are listed under this name. See all Albuterol Sulfate 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 Albuterol Sulfate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Albuterol Sulfate	Albuterol sulfate 108 ug/1	Aerosol, MeteredRespiratory (Inhalation)	REMEDYREPACK INC.	70518-4528	70518-4528-00
Albuterol Sulfate	Albuterol sulfate 90 ug/1	InhalantRespiratory (Inhalation)	Preferred Pharmaceuticals, Inc.	68788-4041	68788-4041-02
Albuterol Sulfate	Albuterol sulfate 90 ug/1	InhalantRespiratory (Inhalation)	REMEDYREPACK INC.	70518-4496	70518-4496-00
Albuterol Sulfate	Albuterol sulfate .83 mg/mL	SolutionRespiratory (Inhalation)	REMEDYREPACK INC.	70518-4490	70518-4490-00
Albuterol sulfate	Albuterol sulfate 90 ug/1	Aerosol, MeteredRespiratory (Inhalation)	Preferred Pharmaceuticals, Inc.	68788-8878	68788-8878-02
Albuterol Sulfate	Albuterol sulfate 90 ug/1	InhalantRespiratory (Inhalation)	Preferred Pharmaceuticals Inc.	68788-8874	68788-8874-02
Albuterol Sulfate	Albuterol sulfate 2.5 mg/.5mL	SolutionRespiratory (Inhalation)	Rising Pharma Holdings, Inc.	64980-642	64980-0642-03
Albuterol Sulfate	Albuterol sulfate .63 mg/3mL	SolutionRespiratory (Inhalation)	Rising Pharma Holdings, Inc	64980-643	64980-0643-03
Albuterol Sulfate	Albuterol sulfate 1.25 mg/3mL	SolutionRespiratory (Inhalation)	Rising Pharma Holdings, Inc	64980-644	64980-0644-02
Albuterol Sulfate	Albuterol sulfate 2.5 mg/3mL	SolutionRespiratory (Inhalation)	Rising Pharma Holdings, Inc.	64980-641	64980-0641-0264980-0641-0364980-0641-06

All 90 Albuterol Sulfate NDCs

Other NDCs under ANDA 072637

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

FDA NDC Directory listings under ANDA 072637
Product	Strength	Form · route	Labeler	Product NDC
albuterol sulfate	Albuterol sulfate 2 mg/1	TabletOral	Golden State Medical Supply, Inc.	51407-367
albuterol sulfate	Albuterol sulfate 4 mg/1	TabletOral	Golden State Medical Supply, Inc.	51407-368
albuterol sulfate	Albuterol sulfate 2 mg/1	TabletOral	Sun Pharmaceutical Industries, Inc.	53489-176
albuterol sulfate	Albuterol sulfate 4 mg/1	TabletOral	Sun Pharmaceutical Industries, Inc.	53489-177