NDC 72189-111 – Ciprofloxacin
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC72189-111
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofloxacin hydrochloride
- Labeler
- DIRECT RX
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077859
- Marketed since
- June 12, 2020
- Marketing end
- February 28, 2027
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 500 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 72189-111-10 | 10 TABLET, FILM COATED in 1 BOTTLE (72189-111-10) | Jun 12, 2020 |
| 72189-111-14 | 14 TABLET, FILM COATED in 1 BOTTLE (72189-111-14) | Jun 12, 2020 |
| 72189-111-20 | 20 TABLET, FILM COATED in 1 BOTTLE (72189-111-20) | Jun 12, 2020 |
| 72189-111-30 | 30 TABLET, FILM COATED in 1 BOTTLE (72189-111-30) | Jun 12, 2020 |
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