NDC 61314-656 – Ciprofloxacin Hydrochloride
Ciprofloxacin Hydrochloride 3 mg/mL · Solution/ Drops · Ophthalmic
Product NDC61314-656
Product details
- Brand name
- Ciprofloxacin Hydrochloride
- Generic name
- Ciprofloxacin Hydrochloride
- Labeler
- Sandoz Inc
- Dosage form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing category
- NDA AUTHORIZED GENERIC · NDA019992
- Marketed since
- May 7, 2004
- Listing expires
- December 31, 2026
- Pharmacologic class
- Quinolone Antimicrobial
Active ingredients
- Ciprofloxacin Hydrochloride 3 mg/mL
Uses, dosage, side effects and warnings for Ciprofloxacin Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 61314-656-05 | 1 BOTTLE, PLASTIC in 1 CARTON (61314-656-05) / 5 mL in 1 BOTTLE, PLASTIC | May 7, 2004 |
| 61314-656-10 | 1 BOTTLE, PLASTIC in 1 CARTON (61314-656-10) / 10 mL in 1 BOTTLE, PLASTIC | May 7, 2004 |
| 61314-656-25 | 1 BOTTLE, PLASTIC in 1 CARTON (61314-656-25) / 2.5 mL in 1 BOTTLE, PLASTIC | May 7, 2004 |
Recalls mentioning this NDC
- D-1044-2022 Jun 15, 2022 · Class II
cGMP deviations: Temperature abuse
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