NDC 0781-6039 – Amoxicillin
Amoxicillin 125 mg/5mL · Powder, For Suspension · Oral
Product NDC0781-6039
Product details
- Brand name
- Amoxicillin
- Generic name
- Amoxicillin
- Labeler
- Sandoz Inc
- Dosage form
- Powder, For Suspension
- Route
- Oral
- Marketing category
- ANDA · ANDA065387
- Marketed since
- March 26, 2007
- Listing expires
- December 31, 2027
- Pharmacologic class
- Penicillin-class Antibacterial
Active ingredients
- Amoxicillin 125 mg/5mL
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 0781-6039-46 | 100 mL in 1 BOTTLE (0781-6039-46) | Mar 26, 2007 |
| 0781-6039-55 | 150 mL in 1 BOTTLE (0781-6039-55) | Mar 26, 2007 |
| 0781-6039-58 | 80 mL in 1 BOTTLE (0781-6039-58) | Mar 26, 2007 |
Recalls mentioning this NDC
- D-0166-2024 Jan 3, 2024 · Class II
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions. - D-1025-2022 Jun 15, 2022 · Class II
cGMP deviations: Temperature abuse - D-268-2013 May 1, 2013 · Class II
Presence of Foreign Substance, Sandoz is recalling certain lots of Amoxicillin Capsules, USP 500 mg due to potential contamination with fragments of stainless steel wire mesh.
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