NDC 0781-5060 – Amoxicillin
Amoxicillin 500 mg/1 · Tablet, Film Coated · Oral
Product NDC0781-5060
Product details
- Brand name
- Amoxicillin
- Generic name
- Amoxicillin
- Labeler
- Sandoz Inc
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA065228
- Marketed since
- July 13, 2005
- Listing expires
- December 31, 2027
- Pharmacologic class
- Penicillin-class Antibacterial
Active ingredients
- Amoxicillin 500 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0781-5060-01 | 100 TABLET, FILM COATED in 1 BOTTLE (0781-5060-01) | Jul 13, 2005 |
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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