NDC 70518-3829 – Famotidine
Famotidine 20 mg/1 · Tablet, Film Coated · Oral
Product NDC70518-3829
Product details
- Brand name
- Famotidine
- Generic name
- Famotidine
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA215630
- Marketed since
- August 15, 2023
- Listing expires
- December 31, 2027
- Pharmacologic class
- Histamine-2 Receptor Antagonist
Active ingredients
- Famotidine 20 mg/1
Package NDC codes (8)
| Package NDC | Description | Since |
|---|---|---|
| 70518-3829-1 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-1) | Nov 6, 2023 |
| 70518-3829-3 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-3) | Jan 24, 2024 |
| 70518-3829-4 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-4) | Feb 28, 2024 |
| 70518-3829-5 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3829-5) | Jun 12, 2024 |
| 70518-3829-6 | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-6) | Nov 21, 2024 |
| 70518-3829-7 | 60 TABLET, FILM COATED in 1 BLISTER PACK (70518-3829-7) | Jan 4, 2025 |
| 70518-3829-8 | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-8) | Jan 14, 2025 |
| 70518-3829-9 | 25 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-9) | Oct 15, 2025 |
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