FDA
Ibuprofen and Famotidine
The FDA lists this product in 7 strengths and forms.
Composition
- Active ingredients
- FAMOTIDINE 26.6MG; IBUPROFEN 800MG
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- FAMOTIDINE 26.6MG; IBUPROFEN 800MG · TabletANDA215925-001 · Discontinued
- FAMOTIDINE 26.6MG; IBUPROFEN 800MG · TabletANDA211890-001 · Prescription
- FAMOTIDINE 26.6MG; IBUPROFEN 800MG · TabletANDA216814-001 · Prescription
- FAMOTIDINE 26.6MG; IBUPROFEN 800MG · TabletANDA219538-001 · Discontinued
- FAMOTIDINE 26.6MG; IBUPROFEN 800MG · TabletThis page
- FAMOTIDINE 26.6MG; IBUPROFEN 800MG · TabletANDA218684-001 · Prescription
- FAMOTIDINE 26.6MG; IBUPROFEN 800MG · TabletANDA203658-001 · Prescription
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application ANDA211278.
At a glance
- Brand name
- Ibuprofen and Famotidine
- Active substance
- famotidine
- Route
- Oral
- Dosage form
- Tablet
- Applicant
- Teva Pharms USA
- Status
- Discontinued
- FDA approval
- 29 Oct 2021
- Application
- ANDA211278-001