NDC 68180-407 – Cefixime
Cefixime 200 mg/5mL · Powder, For Suspension · Oral
Product NDC68180-407
Product details
- Brand name
- Cefixime
- Generic name
- Cefixime
- Labeler
- Lupin Pharmaceuticals, Inc.
- Dosage form
- Powder, For Suspension
- Route
- Oral
- Marketing category
- ANDA · ANDA065355
- Marketed since
- April 24, 2015
- Listing expires
- December 31, 2026
- Pharmacologic class
- Cephalosporin Antibacterial
Active ingredients
- Cefixime 200 mg/5mL
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 68180-407-03 | 50 mL in 1 BOTTLE (68180-407-03) | Apr 24, 2015 |
| 68180-407-04 | 75 mL in 1 BOTTLE (68180-407-04) | Apr 24, 2015 |
Recalls mentioning this NDC
- D-0648-2024 Sep 4, 2024 · Class II
Subpotent Drug- An out of specification ( OOS ) result observed in assay test during 18-month long term stability study. - D-0559-2024 Jun 26, 2024 · Class II
Failed Content Uniformity Specifications - D-0274-2024 Feb 7, 2024 · Class II
Failed Impurities/Degradation Specifications - D-0390-2021 May 26, 2021 · Class II
Subpotent Drug - D-1252-2020 Apr 29, 2020 · Class II
Subpotent Drug: low out of specification (OOS) test result observed in long term stability study.
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