Composition
- Active ingredients
- ALBUTEROL SULFATE EQ 4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- ALBUTEROL SULFATE EQ 4MG BASE · Tablet, extended releaseNDA019383-001 · Discontinued
- ALBUTEROL SULFATE EQ 4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TabletThis page
- ALBUTEROL SULFATE EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TabletNDA017853-001 · Discontinued
- ALBUTEROL SULFATE EQ 2MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · SyrupNDA018062-001 · Discontinued
- ALBUTEROL SULFATE EQ 0.5% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · SolutionNDA019243-001 · Discontinued
- ALBUTEROL SULFATE EQ 0.083% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · SolutionNDA019243-002 · Discontinued
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application NDA017853.
At a glance
- Brand name
- Proventil
- Active substance
- albuterol sulfate
- Route
- Oral
- Dosage form
- Tablet
- Applicant
- Schering
- Status
- Discontinued
- FDA approval
- 7 May 1982
- Application
- NDA017853-002