NDC 72789-108 – Ciprofloxacin
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC72789-108
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofloxacin
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076558
- Marketed since
- June 9, 2004
- Listing expires
- December 31, 2027
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 500 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 72789-108-02 | 2 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-108-02) | Apr 5, 2022 |
| 72789-108-10 | 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-108-10) | Dec 9, 2021 |
| 72789-108-14 | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-108-14) | Jul 21, 2021 |
| 72789-108-20 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-108-20) | Dec 30, 2020 |
| 72789-108-28 | 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-108-28) | May 5, 2022 |
| 72789-108-30 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-108-30) | Dec 9, 2020 |
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