NDC 31722-700 – Losartan Potassium
Losartan Potassium 25 mg/1 · Tablet, Film Coated · Oral
Product NDC31722-700
Product details
- Brand name
- Losartan Potassium
- Generic name
- Losartan Potassium
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA203835
- Marketed since
- August 19, 2015
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin 2 Receptor Blocker
Active ingredients
- Losartan Potassium 25 mg/1
Uses, dosage, side effects and warnings for Losartan potassium →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 31722-700-05 | 500 TABLET, FILM COATED in 1 BOTTLE (31722-700-05) | Aug 19, 2015 |
| 31722-700-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (31722-700-10) | Aug 19, 2015 |
| 31722-700-30 | 30 TABLET, FILM COATED in 1 BOTTLE (31722-700-30) | Aug 19, 2015 |
| 31722-700-60 | 60 TABLET, FILM COATED in 1 BOTTLE (31722-700-60) | Aug 19, 2015 |
| 31722-700-90 | 90 TABLET, FILM COATED in 1 BOTTLE (31722-700-90) | Aug 19, 2015 |
Recalls mentioning this NDC
- D-1043-2019 Mar 27, 2019 · Class II
CGMP Deviations; trace amounts of N-Nitroso N-Methyl 4-amino butyric acid (NMBA) detected in the active pharmaceutical ingredient - D-1042-2019 Mar 27, 2019 · Class II
CGMP Deviations; trace amounts of N-Nitroso N-Methyl 4-amino butyric acid (NMBA) detected in the active pharmaceutical ingredient - D-1041-2019 Mar 27, 2019 · Class II
CGMP Deviations; trace amounts of N-Nitroso N-Methyl 4-amino butyric acid (NMBA) detected in the active pharmaceutical ingredient
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