Proventil Hfa
NDC Package 0085-1132-02
Package Information
Proventil Hfa is pROVENTIL® HFA Inhalation Aerosol is indicated in adults and children 4 years of age and older for the treatment or prevention of bronchospasm with reversible obstructive airway disease and for the prevention of exercise-induced bronchospasm. Marketed by Merck Sharp & Dohme Corp., this product is identified by NDC 0085-1132 and is authorized under FDA application NDA020503.
Identification & Billing
- RxCUI: 2123111 - albuterol 90 MCG/INHAL Metered Dose Inhaler, 200 Actuations, generic for Proventil
- RxCUI: 2123111 - NDA020503 200 ACTUAT albuterol 0.09 MG/ACTUAT Metered Dose Inhaler
- RxCUI: 746763 - Proventil HFA 90 MCG/INHAL Metered Dose Inhaler, 200 Actuations
- RxCUI: 746763 - NDA020503 200 ACTUAT albuterol 0.09 MG/ACTUAT Metered Dose Inhaler [Proventil]
- RxCUI: 746763 - NDA020503 200 ACTUAT Proventil 0.09 MG/ACTUAT Metered Dose Inhaler
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 0085 - Merck Sharp & Dohme Corp.
- 0085-1132 - Proventil Hfa
- 0085-1132-02 - 1 CANISTER in 1 CARTON / 100 AEROSOL, METERED in 1 CANISTER
- 0085-1132 - Proventil Hfa
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
* Please review the full disclaimer at the bottom of this page.
Other Available Packages
The following commercial packages are registered under the same Product NDC (0085-1132). Click a package code to view its specific billing and regulatory data.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 0085-1132-02 identifies a specific commercial package of 1 canister in 1 carton / 100 aerosol, metered in 1 canister of Proventil Hfa, labeled by Merck Sharp & Dohme Corp.. This is formulated for use and contains as the active substance.
Is this product currently listed with the FDA?
This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Merck Sharp & Dohme Corp. on October 01, 2001. The current certification is valid through December 31, 2020.
How is this Merck Sharp & Dohme Corp. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00085113202. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Labeler segment to maintain the 5-4-2 structure.