NDC 85766-221 – Famotidine
Famotidine 20 mg/1 · Tablet, Film Coated · Oral
Product NDC85766-221
Product details
- Brand name
- Famotidine
- Generic name
- Famotidine
- Labeler
- Sportpharm LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA075718
- Marketed since
- April 16, 2001
- Listing expires
- December 31, 2027
- Pharmacologic class
- Histamine-2 Receptor Antagonist
Active ingredients
- Famotidine 20 mg/1
Package NDC codes (9)
| Package NDC | Description | Since |
|---|---|---|
| 85766-221-01 | 100 TABLET, FILM COATED in 1 BOTTLE (85766-221-01) | Jun 26, 2026 |
| 85766-221-07 | 7 TABLET, FILM COATED in 1 BOTTLE (85766-221-07) | Jun 26, 2026 |
| 85766-221-10 | 10 TABLET, FILM COATED in 1 BOTTLE (85766-221-10) | Jun 26, 2026 |
| 85766-221-14 | 14 TABLET, FILM COATED in 1 BOTTLE (85766-221-14) | Jun 26, 2026 |
| 85766-221-15 | 15 TABLET, FILM COATED in 1 BOTTLE (85766-221-15) | Jun 26, 2026 |
| 85766-221-20 | 20 TABLET, FILM COATED in 1 BOTTLE (85766-221-20) | Jun 26, 2026 |
| 85766-221-30 | 30 TABLET, FILM COATED in 1 BOTTLE (85766-221-30) | Jun 26, 2026 |
| 85766-221-60 | 60 TABLET, FILM COATED in 1 BOTTLE (85766-221-60) | Jun 26, 2026 |
| 85766-221-90 | 90 TABLET, FILM COATED in 1 BOTTLE (85766-221-90) | Jun 26, 2026 |
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