NDC 60760-937 – Famotidine
Famotidine 40 mg/1 · Tablet, Film Coated · Oral
Product NDC60760-937
Product details
- Brand name
- Famotidine
- Generic name
- Famotidine
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA215767
- Marketed since
- March 28, 2025
- Listing expires
- December 31, 2027
- Pharmacologic class
- Histamine-2 Receptor Antagonist
Active ingredients
- Famotidine 40 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 60760-937-07 | 7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-937-07) | Mar 28, 2025 |
| 60760-937-60 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-937-60) | May 22, 2025 |
Other Famotidine products
- 50090-6790 Famotidine 40 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-6916 Famotidine 40 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-7829 Famotidine 20 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-6932 Famotidine 20 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-1044 Famotidine 20 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-6582 Famotidine 20 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-7982 Famotidine 40 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-7180 Famotidine 20 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-7178 Famotidine 20 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-7981 Famotidine 40 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-7196 Famotidine 40 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 80425-0589 Famotidine 20 mg/1 · Tablet, Film Coated · Advanced Rx of Tennessee, LLC