NDC 70000-0049 – Famotidine
Famotidine 20 mg/1 · Tablet, Film Coated · Oral
Product NDC70000-0049
Product details
- Brand name
- Famotidine
- Generic name
- Famotidine
- Labeler
- LEADER/ CARDINAL HEALTH 110, INC.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA206531
- Marketed since
- April 4, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Histamine-2 Receptor Antagonist
Active ingredients
- Famotidine 20 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 70000-0049-1 | 1 BOTTLE in 1 CARTON (70000-0049-1) / 25 TABLET, FILM COATED in 1 BOTTLE | Apr 4, 2020 |
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