FDA
Nalidixic Acid
The FDA lists this product in 6 strengths and forms.
Composition
- Active ingredients
- NALIDIXIC ACID 250MG
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- NALIDIXIC ACID 250MG · TabletThis page
- NALIDIXIC ACID 500MG · TabletANDA070271-001 · Discontinued
- NALIDIXIC ACID 250MG · TabletANDA071936-001 · Discontinued
- NALIDIXIC ACID 500MG · TabletANDA072061-001 · Discontinued
- NALIDIXIC ACID 1GM · TabletANDA070272-001 · Discontinued
- NALIDIXIC ACID 1GM · TabletANDA071919-001 · Discontinued
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application ANDA070270.
Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.
At a glance
- Brand name
- Nalidixic Acid
- Route
- Oral
- Dosage form
- Tablet
- Applicant
- Sun Pharm Industries
- Status
- Discontinued
- FDA approval
- 28 Mar 1986
- Application
- ANDA070270-001