Drug company (FDA labeler)
Ritedose Pharmaceuticals, LLC
NDC labeler code: 76204
What is a labeler?
The company whose name is on the package and in the FDA’s National Drug Code (NDC) Directory. It may make the medicine itself or sell medicine made by another company. The first part of every NDC code identifies the labeler.
Official FDA data only
Products, approvals and recalls come from the FDA (NDC Directory, Drugs@FDA, enforcement reports). Recalls are linked to this company by the NDC labeler code on the recalled product.
Questions about your medicine: ask your doctor or pharmacist. In an emergency, call 911.
Prescription medicines
- Albuterol sulfateVentolin HFA, Albuterol Sulate HFA, Proair Respiclick · 4 products
- LevalbuterolXopenex HFA · 3 products
- Arformoterol tartrate1 product
- Ipratropium bromide and albuterol sulfateCombivent Respimat · 1 product
- TobramycinTobramycin Inhalation Solution Pak, Tobi, Tobi Podhaler · 1 product
- Ipratropium bromideAtrovent HFA · 1 product
- Formoterol fumaratePerforomist · 1 product
FDA applications for these products
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Approved | Application | Medicine | Sponsor |
|---|---|---|---|
| March 12, 2025 | ANDA218386 | Albuterol sulfate ALBUTEROL SULFATE | Ritedose Corp |
| November 25, 2022 | ANDA216486 | Formoterol fumarate FORMOTEROL FUMARATE | Ritedose Corp |
| March 2, 2022 | ANDA214736 | Arformoterol tartrate ARFORMOTEROL TARTRATE | Ritedose Corp |
| December 28, 2021 | ANDA214531 | Albuterol sulfate ALBUTEROL SULFATE | Ritedose Corp |
| March 22, 2016 | ANDA203653 | Levalbuterol LEVALBUTEROL HYDROCHLORIDE | Ritedose Corp |
| May 28, 2014 | ANDA201422 | Tobramycin TOBRAMYCIN | Hikma |
| October 1, 2012 | ANDA202496 | Ipratropium bromide and albuterol sulfate ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE | Ritedose Corp |
| December 16, 2008 | ANDA077839 | Albuterol sulfate ALBUTEROL SULFATE | Ritedose Corp |
| January 26, 2001 | ANDA075693 | Ipratropium bromide IPRATROPIUM BROMIDE | Ritedose Corp |
The sponsor is the company that holds the FDA application; it can differ from the labeler.
Recall timeline
No recall of these products (by NDC code) appears in the FDA enforcement reports.
Next steps
- Find a pharmacy near youAsk which company made your medicine and whether it is recalled
- Latest FDA drug recallsAll companies, newest first
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- All prescription drugs A to ZSearch by generic, brand or Spanish name
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026