51655-116-52 |
51655-116 |
HUMAN PRESCRIPTION DRUG |
Escitalopram |
Escitalopram |
TABLET, FILM COATED |
ORAL |
20220711 |
N/A |
ANDA |
ANDA078032 |
Northwind Pharmaceuticals, LLC |
ESCITALOPRAM OXALATE |
5 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-116-52) |
42708-155-30 |
42708-155 |
HUMAN PRESCRIPTION DRUG |
Escitalopram |
Escitalopram |
TABLET, FILM COATED |
ORAL |
20220804 |
N/A |
ANDA |
ANDA078032 |
QPharma Inc |
ESCITALOPRAM OXALATE |
10 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (42708-155-30) |
42708-163-30 |
42708-163 |
HUMAN PRESCRIPTION DRUG |
Escitalopram |
Escitalopram |
TABLET, FILM COATED |
ORAL |
20230313 |
N/A |
ANDA |
ANDA078032 |
QPharma Inc |
ESCITALOPRAM OXALATE |
20 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-163-30) |
50090-5312-0 |
50090-5312 |
HUMAN PRESCRIPTION DRUG |
Escitalopram |
Escitalopram |
TABLET, FILM COATED |
ORAL |
20201029 |
N/A |
ANDA |
ANDA078032 |
A-S Medication Solutions |
ESCITALOPRAM OXALATE |
5 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (50090-5312-0) |
50090-5312-1 |
50090-5312 |
HUMAN PRESCRIPTION DRUG |
Escitalopram |
Escitalopram |
TABLET, FILM COATED |
ORAL |
20230713 |
N/A |
ANDA |
ANDA078032 |
A-S Medication Solutions |
ESCITALOPRAM OXALATE |
5 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (50090-5312-1) |
50090-6190-0 |
50090-6190 |
HUMAN PRESCRIPTION DRUG |
Escitalopram |
Escitalopram |
TABLET, FILM COATED |
ORAL |
20221028 |
N/A |
ANDA |
ANDA078032 |
A-S Medication Solutions |
ESCITALOPRAM OXALATE |
10 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (50090-6190-0) |
50090-6190-1 |
50090-6190 |
HUMAN PRESCRIPTION DRUG |
Escitalopram |
Escitalopram |
TABLET, FILM COATED |
ORAL |
20221028 |
N/A |
ANDA |
ANDA078032 |
A-S Medication Solutions |
ESCITALOPRAM OXALATE |
10 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (50090-6190-1) |
50090-6191-0 |
50090-6191 |
HUMAN PRESCRIPTION DRUG |
Escitalopram |
Escitalopram |
TABLET, FILM COATED |
ORAL |
20221028 |
N/A |
ANDA |
ANDA078032 |
A-S Medication Solutions |
ESCITALOPRAM OXALATE |
10 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (50090-6191-0) |
51655-277-26 |
51655-277 |
HUMAN PRESCRIPTION DRUG |
Escitalopram |
Escitalopram |
TABLET, FILM COATED |
ORAL |
20221005 |
N/A |
ANDA |
ANDA078032 |
Northwind Pharmaceuticals, LLC |
ESCITALOPRAM OXALATE |
10 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-277-26) |
51655-277-52 |
51655-277 |
HUMAN PRESCRIPTION DRUG |
Escitalopram |
Escitalopram |
TABLET, FILM COATED |
ORAL |
20220908 |
N/A |
ANDA |
ANDA078032 |
Northwind Pharmaceuticals, LLC |
ESCITALOPRAM OXALATE |
10 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-277-52) |
51655-284-26 |
51655-284 |
HUMAN PRESCRIPTION DRUG |
Escitalopram |
Escitalopram |
TABLET, FILM COATED |
ORAL |
20200513 |
N/A |
ANDA |
ANDA078032 |
Northwind Pharmaceuticals |
ESCITALOPRAM OXALATE |
20 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-284-26) |
51655-284-52 |
51655-284 |
HUMAN PRESCRIPTION DRUG |
Escitalopram |
Escitalopram |
TABLET, FILM COATED |
ORAL |
20220720 |
N/A |
ANDA |
ANDA078032 |
Northwind Pharmaceuticals |
ESCITALOPRAM OXALATE |
20 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-284-52) |
53002-2438-0 |
53002-2438 |
HUMAN PRESCRIPTION DRUG |
Escitalopram |
Escitalopram |
TABLET, FILM COATED |
ORAL |
20220501 |
N/A |
ANDA |
ANDA078032 |
RPK Pharmaceuticals, Inc. |
ESCITALOPRAM OXALATE |
10 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (53002-2438-0) |
53002-2438-3 |
53002-2438 |
HUMAN PRESCRIPTION DRUG |
Escitalopram |
Escitalopram |
TABLET, FILM COATED |
ORAL |
20220501 |
N/A |
ANDA |
ANDA078032 |
RPK Pharmaceuticals, Inc. |
ESCITALOPRAM OXALATE |
10 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (53002-2438-3) |
53002-2438-6 |
53002-2438 |
HUMAN PRESCRIPTION DRUG |
Escitalopram |
Escitalopram |
TABLET, FILM COATED |
ORAL |
20220501 |
N/A |
ANDA |
ANDA078032 |
RPK Pharmaceuticals, Inc. |
ESCITALOPRAM OXALATE |
10 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (53002-2438-6) |
53002-5453-0 |
53002-5453 |
HUMAN PRESCRIPTION DRUG |
Escitalopram |
Escitalopram |
TABLET, FILM COATED |
ORAL |
20230101 |
N/A |
ANDA |
ANDA078032 |
RPK Pharmaceuticals, Inc. |
ESCITALOPRAM OXALATE |
20 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (53002-5453-0) |
53002-5453-3 |
53002-5453 |
HUMAN PRESCRIPTION DRUG |
Escitalopram |
Escitalopram |
TABLET, FILM COATED |
ORAL |
20230101 |
N/A |
ANDA |
ANDA078032 |
RPK Pharmaceuticals, Inc. |
ESCITALOPRAM OXALATE |
20 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (53002-5453-3) |
53002-5453-6 |
53002-5453 |
HUMAN PRESCRIPTION DRUG |
Escitalopram |
Escitalopram |
TABLET, FILM COATED |
ORAL |
20230101 |
N/A |
ANDA |
ANDA078032 |
RPK Pharmaceuticals, Inc. |
ESCITALOPRAM OXALATE |
20 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (53002-5453-6) |
55700-818-30 |
55700-818 |
HUMAN PRESCRIPTION DRUG |
Escitalopram |
Escitalopram |
TABLET, FILM COATED |
ORAL |
20191114 |
N/A |
ANDA |
ANDA078032 |
Quality Care Products, LLC |
ESCITALOPRAM OXALATE |
20 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (55700-818-30) |
55700-818-90 |
55700-818 |
HUMAN PRESCRIPTION DRUG |
Escitalopram |
Escitalopram |
TABLET, FILM COATED |
ORAL |
20191114 |
N/A |
ANDA |
ANDA078032 |
Quality Care Products, LLC |
ESCITALOPRAM OXALATE |
20 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (55700-818-90) |