| 68788-9368-1 |
68788-9368 |
HUMAN PRESCRIPTION DRUG |
Ondansetron Hydrochloride |
Ondansetron Hydrochloride |
TABLET, FILM COATED |
ORAL |
20120612 |
N/A |
ANDA |
ANDA078539 |
Preferred Pharmaceuticals, Inc. |
ONDANSETRON HYDROCHLORIDE |
4 mg/1 |
10 TABLET, FILM COATED in 1 BOTTLE (68788-9368-1) |
| 68788-9368-2 |
68788-9368 |
HUMAN PRESCRIPTION DRUG |
Ondansetron Hydrochloride |
Ondansetron Hydrochloride |
TABLET, FILM COATED |
ORAL |
20170623 |
N/A |
ANDA |
ANDA078539 |
Preferred Pharmaceuticals, Inc. |
ONDANSETRON HYDROCHLORIDE |
4 mg/1 |
12 TABLET, FILM COATED in 1 BOTTLE (68788-9368-2) |
| 68788-9368-3 |
68788-9368 |
HUMAN PRESCRIPTION DRUG |
Ondansetron Hydrochloride |
Ondansetron Hydrochloride |
TABLET, FILM COATED |
ORAL |
20120612 |
N/A |
ANDA |
ANDA078539 |
Preferred Pharmaceuticals, Inc. |
ONDANSETRON HYDROCHLORIDE |
4 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (68788-9368-3) |
| 83008-074-20 |
83008-074 |
HUMAN PRESCRIPTION DRUG |
Ondansetron Hydrochloride |
Ondansetron Hydrochloride |
TABLET, FILM COATED |
ORAL |
20240725 |
20280131 |
ANDA |
ANDA078539 |
Quality Care Products, LLC |
ONDANSETRON HYDROCHLORIDE |
4 mg/1 |
20 TABLET, FILM COATED in 1 BOTTLE (83008-074-20) |
| 83008-074-30 |
83008-074 |
HUMAN PRESCRIPTION DRUG |
Ondansetron Hydrochloride |
Ondansetron Hydrochloride |
TABLET, FILM COATED |
ORAL |
20240725 |
20280131 |
ANDA |
ANDA078539 |
Quality Care Products, LLC |
ONDANSETRON HYDROCHLORIDE |
4 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (83008-074-30) |
| 50268-621-15 |
50268-621 |
HUMAN PRESCRIPTION DRUG |
Ondansetron Hydrochloride |
Ondansetron Hydrochloride |
TABLET, FILM COATED |
ORAL |
20160805 |
N/A |
ANDA |
ANDA078539 |
AvPAK |
ONDANSETRON HYDROCHLORIDE |
4 mg/1 |
50 BLISTER PACK in 1 BOX (50268-621-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-621-11) |
| 70518-1585-0 |
70518-1585 |
HUMAN PRESCRIPTION DRUG |
Ondansetron Hydrochloride |
Ondansetron Hydrochloride |
TABLET, FILM COATED |
ORAL |
20181024 |
N/A |
ANDA |
ANDA078539 |
REMEDYREPACK INC. |
ONDANSETRON HYDROCHLORIDE |
4 mg/1 |
30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1585-0) |
| 70518-1585-6 |
70518-1585 |
HUMAN PRESCRIPTION DRUG |
Ondansetron Hydrochloride |
Ondansetron Hydrochloride |
TABLET, FILM COATED |
ORAL |
20251001 |
N/A |
ANDA |
ANDA078539 |
REMEDYREPACK INC. |
ONDANSETRON HYDROCHLORIDE |
4 mg/1 |
20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1585-6) |
| 51655-933-04 |
51655-933 |
HUMAN PRESCRIPTION DRUG |
Ondansetron Hydrochloride |
Ondansetron Hydrochloride |
TABLET, FILM COATED |
ORAL |
20221025 |
N/A |
ANDA |
ANDA078539 |
Northwind Health Company, LLC |
ONDANSETRON HYDROCHLORIDE |
4 mg/1 |
4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-04) |
| 42708-059-05 |
42708-059 |
HUMAN PRESCRIPTION DRUG |
Ondansetron Hydrochloride |
Ondansetron Hydrochloride |
TABLET, FILM COATED |
ORAL |
20180419 |
N/A |
ANDA |
ANDA078539 |
QPharma, Inc. |
ONDANSETRON HYDROCHLORIDE |
8 mg/1 |
5 TABLET, FILM COATED in 1 BOTTLE (42708-059-05) |
| 76420-917-01 |
76420-917 |
HUMAN PRESCRIPTION DRUG |
Ondansetron Hydrochloride |
Ondansetron Hydrochloride |
TABLET, FILM COATED |
ORAL |
20250128 |
N/A |
ANDA |
ANDA078539 |
Asclemed USA, Inc. |
ONDANSETRON HYDROCHLORIDE |
24 mg/1 |
1 BLISTER PACK in 1 CARTON (76420-917-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK |
| 57237-076-30 |
57237-076 |
HUMAN PRESCRIPTION DRUG |
Ondansetron Hydrochloride |
Ondansetron Hydrochloride |
TABLET, FILM COATED |
ORAL |
20070731 |
N/A |
ANDA |
ANDA078539 |
Rising Pharma Holdings, Inc. |
ONDANSETRON HYDROCHLORIDE |
8 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (57237-076-30) |
| 57237-076-50 |
57237-076 |
HUMAN PRESCRIPTION DRUG |
Ondansetron Hydrochloride |
Ondansetron Hydrochloride |
TABLET, FILM COATED |
ORAL |
20221004 |
N/A |
ANDA |
ANDA078539 |
Rising Pharma Holdings, Inc. |
ONDANSETRON HYDROCHLORIDE |
8 mg/1 |
500 TABLET, FILM COATED in 1 BOTTLE (57237-076-50) |
| 50090-6342-0 |
50090-6342 |
HUMAN PRESCRIPTION DRUG |
Ondansetron Hydrochloride |
Ondansetron Hydrochloride |
TABLET, FILM COATED |
ORAL |
20230123 |
N/A |
ANDA |
ANDA078539 |
A-S Medication Solutions |
ONDANSETRON HYDROCHLORIDE |
4 mg/1 |
10 TABLET, FILM COATED in 1 BOTTLE (50090-6342-0) |
| 50090-6342-1 |
50090-6342 |
HUMAN PRESCRIPTION DRUG |
Ondansetron Hydrochloride |
Ondansetron Hydrochloride |
TABLET, FILM COATED |
ORAL |
20230123 |
N/A |
ANDA |
ANDA078539 |
A-S Medication Solutions |
ONDANSETRON HYDROCHLORIDE |
4 mg/1 |
6 TABLET, FILM COATED in 1 BOTTLE (50090-6342-1) |
| 50090-6342-2 |
50090-6342 |
HUMAN PRESCRIPTION DRUG |
Ondansetron Hydrochloride |
Ondansetron Hydrochloride |
TABLET, FILM COATED |
ORAL |
20230123 |
N/A |
ANDA |
ANDA078539 |
A-S Medication Solutions |
ONDANSETRON HYDROCHLORIDE |
4 mg/1 |
20 TABLET, FILM COATED in 1 BOTTLE (50090-6342-2) |
| 50090-6342-4 |
50090-6342 |
HUMAN PRESCRIPTION DRUG |
Ondansetron Hydrochloride |
Ondansetron Hydrochloride |
TABLET, FILM COATED |
ORAL |
20230123 |
N/A |
ANDA |
ANDA078539 |
A-S Medication Solutions |
ONDANSETRON HYDROCHLORIDE |
4 mg/1 |
3 TABLET, FILM COATED in 1 BOTTLE (50090-6342-4) |
| 50090-6342-5 |
50090-6342 |
HUMAN PRESCRIPTION DRUG |
Ondansetron Hydrochloride |
Ondansetron Hydrochloride |
TABLET, FILM COATED |
ORAL |
20230123 |
N/A |
ANDA |
ANDA078539 |
A-S Medication Solutions |
ONDANSETRON HYDROCHLORIDE |
4 mg/1 |
12 TABLET, FILM COATED in 1 BOTTLE (50090-6342-5) |
| 42708-044-05 |
42708-044 |
HUMAN PRESCRIPTION DRUG |
Ondansetron Hydrochloride |
Ondansetron Hydrochloride |
TABLET, FILM COATED |
ORAL |
20180405 |
N/A |
ANDA |
ANDA078539 |
QPharma, Inc. |
ONDANSETRON HYDROCHLORIDE |
4 mg/1 |
5 TABLET, FILM COATED in 1 BOTTLE (42708-044-05) |
| 76420-916-00 |
76420-916 |
HUMAN PRESCRIPTION DRUG |
Ondansetron Hydrochloride |
Ondansetron Hydrochloride |
TABLET, FILM COATED |
ORAL |
20250128 |
N/A |
ANDA |
ANDA078539 |
Asclemed USA, Inc. |
ONDANSETRON HYDROCHLORIDE |
8 mg/1 |
1000 TABLET, FILM COATED in 1 BOTTLE (76420-916-00) |