NDC 25000-086 – Famotidine 10 mg
Famotidine 10 mg/1 · Tablet, Coated · Oral
Product NDC25000-086
Product details
- Brand name
- Famotidine 10 mg
- Generic name
- Famotidine 10 mg
- Labeler
- MARKSANS PHARMA LIMITED
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA217543
- Marketed since
- March 10, 2023
- Listing expires
- December 31, 2026
- Pharmacologic class
- Histamine-2 Receptor Antagonist
Active ingredients
- Famotidine 10 mg/1
Uses, dosage, side effects and warnings for Famotidine 10 mg →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 25000-086-03 | 1 BOTTLE in 1 CARTON (25000-086-03) / 30 TABLET, COATED in 1 BOTTLE | Mar 10, 2023 |
| 25000-086-07 | 1 BOTTLE in 1 CARTON (25000-086-07) / 90 TABLET, COATED in 1 BOTTLE | Apr 24, 2024 |
| 25000-086-08 | 1 BOTTLE in 1 CARTON (25000-086-08) / 100 TABLET, COATED in 1 BOTTLE | Mar 10, 2023 |
| 25000-086-36 | 3 BLISTER PACK in 1 CARTON (25000-086-36) / 10 TABLET, COATED in 1 BLISTER PACK | Mar 10, 2023 |