NDC 43063-869 – Ciprofloxacin
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet · Oral
Product NDC43063-869
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofloxacin
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076639
- Marketed since
- September 10, 2004
- Listing expires
- December 31, 2026
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 500 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 43063-869-06 | 6 TABLET in 1 BOTTLE, PLASTIC (43063-869-06) | Aug 4, 2018 |
| 43063-869-08 | 8 TABLET in 1 BOTTLE, PLASTIC (43063-869-08) | Jul 11, 2018 |
| 43063-869-10 | 10 TABLET in 1 BOTTLE, PLASTIC (43063-869-10) | Aug 22, 2018 |
| 43063-869-20 | 20 TABLET in 1 BOTTLE, PLASTIC (43063-869-20) | Aug 17, 2018 |
| 43063-869-30 | 30 TABLET in 1 BOTTLE, PLASTIC (43063-869-30) | Aug 17, 2018 |
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