NDC 0093-1177 – Neomycin Sulfate
Neomycin Sulfate 500 mg/1 · Tablet · Oral
Product NDC0093-1177
Product details
- Brand name
- Neomycin Sulfate
- Generic name
- Neomycin Sulfate
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA060304
- Marketed since
- September 30, 1990
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aminoglycoside Antibacterial
Active ingredients
- Neomycin Sulfate 500 mg/1
Uses, dosage, side effects and warnings for Neomycin Sulfate →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0093-1177-01 | 100 TABLET in 1 BOTTLE (0093-1177-01) | Sep 30, 1990 |
Recalls mentioning this NDC
- D-1473-2022 Sep 7, 2022 · Class II
CGMP Deviations: A foreign matter identified as teflon was found in the Active Pharmaceutical Ingredient (API) used in the manufacture of Neomycin Sulfate Tablets, USP 500 mg. - D-0574-2021 Jun 2, 2021 · Class II
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Other Neomycin Sulfate products
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- 73473-901 Neomycin Sulfate 500 mg/1 · Tablet · Solaris Pharma Corporation
- 87236-017 Neomycin Sulfate 5 mg/100g · Ointment · Aldermed Inc.
- 87879-003 Neomycin Sulfate 100 kg/100kg · Granule · Shaanxi Shuvita Biotech Co., Ltd