| 70518-4229-2 |
70518-4229 |
HUMAN PRESCRIPTION DRUG |
Ciprofloxacin |
Ciprofolxacin |
TABLET |
ORAL |
20250114 |
N/A |
ANDA |
ANDA208921 |
REMEDYREPACK INC. |
CIPROFLOXACIN HYDROCHLORIDE |
500 mg/1 |
20 TABLET in 1 BOTTLE, PLASTIC (70518-4229-2) |
| 70518-4229-3 |
70518-4229 |
HUMAN PRESCRIPTION DRUG |
Ciprofloxacin |
Ciprofolxacin |
TABLET |
ORAL |
20250129 |
N/A |
ANDA |
ANDA208921 |
REMEDYREPACK INC. |
CIPROFLOXACIN HYDROCHLORIDE |
500 mg/1 |
30 TABLET in 1 BLISTER PACK (70518-4229-3) |
| 70518-4229-4 |
70518-4229 |
HUMAN PRESCRIPTION DRUG |
Ciprofloxacin |
Ciprofolxacin |
TABLET |
ORAL |
20250519 |
N/A |
ANDA |
ANDA208921 |
REMEDYREPACK INC. |
CIPROFLOXACIN HYDROCHLORIDE |
500 mg/1 |
14 TABLET in 1 BLISTER PACK (70518-4229-4) |
| 70518-4229-5 |
70518-4229 |
HUMAN PRESCRIPTION DRUG |
Ciprofloxacin |
Ciprofolxacin |
TABLET |
ORAL |
20250709 |
N/A |
ANDA |
ANDA208921 |
REMEDYREPACK INC. |
CIPROFLOXACIN HYDROCHLORIDE |
500 mg/1 |
14 TABLET in 1 BOTTLE, PLASTIC (70518-4229-5) |
| 70518-4229-6 |
70518-4229 |
HUMAN PRESCRIPTION DRUG |
Ciprofloxacin |
Ciprofolxacin |
TABLET |
ORAL |
20250731 |
N/A |
ANDA |
ANDA208921 |
REMEDYREPACK INC. |
CIPROFLOXACIN HYDROCHLORIDE |
500 mg/1 |
30 TABLET in 1 BLISTER PACK (70518-4229-6) |
| 70518-4229-7 |
70518-4229 |
HUMAN PRESCRIPTION DRUG |
Ciprofloxacin |
Ciprofolxacin |
TABLET |
ORAL |
20260126 |
N/A |
ANDA |
ANDA208921 |
REMEDYREPACK INC. |
CIPROFLOXACIN HYDROCHLORIDE |
500 mg/1 |
30 TABLET in 1 BOTTLE, PLASTIC (70518-4229-7) |
| 68071-3699-1 |
68071-3699 |
HUMAN PRESCRIPTION DRUG |
Ciprofloxacin |
Ciprofolxacin |
TABLET |
ORAL |
20250801 |
N/A |
ANDA |
ANDA208921 |
NuCare Pharmaceutical, Inc. |
CIPROFLOXACIN HYDROCHLORIDE |
250 mg/1 |
10 TABLET in 1 BOTTLE (68071-3699-1) |
| 68071-3699-2 |
68071-3699 |
HUMAN PRESCRIPTION DRUG |
Ciprofloxacin |
Ciprofolxacin |
TABLET |
ORAL |
20251219 |
N/A |
ANDA |
ANDA208921 |
NuCare Pharmaceutical, Inc. |
CIPROFLOXACIN HYDROCHLORIDE |
250 mg/1 |
20 TABLET in 1 BOTTLE (68071-3699-2) |
| 68071-3699-3 |
68071-3699 |
HUMAN PRESCRIPTION DRUG |
Ciprofloxacin |
Ciprofolxacin |
TABLET |
ORAL |
20241014 |
N/A |
ANDA |
ANDA208921 |
NuCare Pharmaceutical, Inc. |
CIPROFLOXACIN HYDROCHLORIDE |
250 mg/1 |
30 TABLET in 1 BOTTLE (68071-3699-3) |
| 68071-3699-6 |
68071-3699 |
HUMAN PRESCRIPTION DRUG |
Ciprofloxacin |
Ciprofolxacin |
TABLET |
ORAL |
20241211 |
N/A |
ANDA |
ANDA208921 |
NuCare Pharmaceutical, Inc. |
CIPROFLOXACIN HYDROCHLORIDE |
250 mg/1 |
6 TABLET in 1 BOTTLE (68071-3699-6) |
| 58657-675-01 |
58657-675 |
HUMAN PRESCRIPTION DRUG |
Ciprofloxacin |
Ciprofloxacin |
TABLET, COATED |
ORAL |
20200812 |
N/A |
ANDA |
ANDA208921 |
Method Pharmaceuticals, LLC |
CIPROFLOXACIN HYDROCHLORIDE |
250 mg/1 |
100 TABLET, COATED in 1 BOTTLE (58657-675-01) |
| 68071-2384-6 |
68071-2384 |
HUMAN PRESCRIPTION DRUG |
Ciprofloxacin |
Ciprofloxacin |
TABLET, COATED |
ORAL |
20210409 |
N/A |
ANDA |
ANDA208921 |
NuCare Pharmaceuticals,Inc. |
CIPROFLOXACIN HYDROCHLORIDE |
500 mg/1 |
60 TABLET, COATED in 1 BOTTLE (68071-2384-6) |
| 68071-2384-7 |
68071-2384 |
HUMAN PRESCRIPTION DRUG |
Ciprofloxacin |
Ciprofloxacin |
TABLET, COATED |
ORAL |
20210409 |
N/A |
ANDA |
ANDA208921 |
NuCare Pharmaceuticals,Inc. |
CIPROFLOXACIN HYDROCHLORIDE |
500 mg/1 |
21 TABLET, COATED in 1 BOTTLE (68071-2384-7) |
| 68071-2384-8 |
68071-2384 |
HUMAN PRESCRIPTION DRUG |
Ciprofloxacin |
Ciprofloxacin |
TABLET, COATED |
ORAL |
20210409 |
N/A |
ANDA |
ANDA208921 |
NuCare Pharmaceuticals,Inc. |
CIPROFLOXACIN HYDROCHLORIDE |
500 mg/1 |
28 TABLET, COATED in 1 BOTTLE (68071-2384-8) |
| 43547-688-10 |
43547-688 |
HUMAN PRESCRIPTION DRUG |
Ciprofloxacin |
Ciprofolxacin |
TABLET |
ORAL |
20231001 |
N/A |
ANDA |
ANDA208921 |
Solco Healthcare US, LLC |
CIPROFLOXACIN HYDROCHLORIDE |
250 mg/1 |
100 TABLET in 1 BOTTLE (43547-688-10) |
| 68071-2383-8 |
68071-2383 |
HUMAN PRESCRIPTION DRUG |
Ciprofloxacin |
Ciprofloxacin |
TABLET, COATED |
ORAL |
20210406 |
N/A |
ANDA |
ANDA208921 |
NuCare Pharmaceuticals,Inc. |
CIPROFLOXACIN HYDROCHLORIDE |
250 mg/1 |
28 TABLET, COATED in 1 BOTTLE (68071-2383-8) |
| 68071-2383-9 |
68071-2383 |
HUMAN PRESCRIPTION DRUG |
Ciprofloxacin |
Ciprofloxacin |
TABLET, COATED |
ORAL |
20210406 |
N/A |
ANDA |
ANDA208921 |
NuCare Pharmaceuticals,Inc. |
CIPROFLOXACIN HYDROCHLORIDE |
250 mg/1 |
90 TABLET, COATED in 1 BOTTLE (68071-2383-9) |
| 68071-3693-6 |
68071-3693 |
HUMAN PRESCRIPTION DRUG |
Ciprofloxacin |
Ciprofolxacin |
TABLET |
ORAL |
20241002 |
N/A |
ANDA |
ANDA208921 |
NuCare Pharmaceuticals, Inc. |
CIPROFLOXACIN HYDROCHLORIDE |
250 mg/1 |
6 TABLET in 1 BOTTLE (68071-3693-6) |
| 71335-2054-0 |
71335-2054 |
HUMAN PRESCRIPTION DRUG |
Ciprofloxacin |
Ciprofloxacin |
TABLET, COATED |
ORAL |
20240403 |
N/A |
ANDA |
ANDA208921 |
Bryant Ranch Prepack |
CIPROFLOXACIN HYDROCHLORIDE |
500 mg/1 |
7 TABLET, COATED in 1 BOTTLE (71335-2054-0) |
| 71335-2054-1 |
71335-2054 |
HUMAN PRESCRIPTION DRUG |
Ciprofloxacin |
Ciprofloxacin |
TABLET, COATED |
ORAL |
20230320 |
N/A |
ANDA |
ANDA208921 |
Bryant Ranch Prepack |
CIPROFLOXACIN HYDROCHLORIDE |
500 mg/1 |
14 TABLET, COATED in 1 BOTTLE (71335-2054-1) |