Caraco Pharmaceutical Laboratories, Ltd.
FDA Approved Drugs
Caraco Pharmaceutical Laboratories, Ltd.
FDA Approved Drugs Database
FDA approved drug product records including application numbers, product numbers, drug names, active ingredients, dosage forms, strengths, approval dates and regulatory status.
- Total Records 17
- Latest Approval Date Dec 23, 2008
- Data Source FDA
- First Approval Date Jan 01, 1982
Company Overview
Company
Caraco Pharmaceutical Laboratories, Ltd.
Country
U.S.A
Website
Social Profiles
Company Snapshot
Caraco Pharmaceutical Laboratories, Ltd.
1150 Elijah McCoy Drive, Detroit, MI 48202
U.S.A
www.caraco.com/ Sales@sunpharmausa.com View on MapFDA Approved Drug Records ( 17 records )
Drug Name
ESCITALOPRAM OXALATE
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
-
Active Ingredient
ESCITALOPRAM OXALATE
Application Number
78219
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ESCITALOPRAM OXALATE
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
-
Active Ingredient
ESCITALOPRAM OXALATE
Application Number
78219
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ESCITALOPRAM OXALATE
Product Number
3
Dosage Form
-
Strength
20MG
Approval Date
-
Active Ingredient
ESCITALOPRAM OXALATE
Application Number
78219
Product Number
3
Dosage Form
-
Strength
20MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
2008-12-23
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Application Number
90265
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
2008-12-23
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
500MG;7.5MG
Approval Date
2008-12-23
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Application Number
90265
Product Number
2
Dosage Form
-
Strength
500MG;7.5MG
Approval Date
2008-12-23
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
500MG;10MG
Approval Date
2008-12-23
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Application Number
90265
Product Number
3
Dosage Form
-
Strength
500MG;10MG
Approval Date
2008-12-23
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;7.5MG
Approval Date
2008-12-23
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Application Number
90380
Product Number
1
Dosage Form
-
Strength
650MG;7.5MG
Approval Date
2008-12-23
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
650MG;10MG
Approval Date
2008-12-23
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Application Number
90380
Product Number
2
Dosage Form
-
Strength
650MG;10MG
Approval Date
2008-12-23
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
660MG;10MG
Approval Date
2008-12-23
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Application Number
90380
Product Number
3
Dosage Form
-
Strength
660MG;10MG
Approval Date
2008-12-23
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
4
Dosage Form
-
Strength
750MG;7.5MG
Approval Date
2008-12-23
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Application Number
90380
Product Number
4
Dosage Form
-
Strength
750MG;7.5MG
Approval Date
2008-12-23
Regulatory Status
Discontinued
Drug Name
LAMOTRIGINE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
-
Active Ingredient
LAMOTRIGINE
Application Number
77757
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
LAMOTRIGINE
Product Number
2
Dosage Form
-
Strength
100MG
Approval Date
-
Active Ingredient
LAMOTRIGINE
Application Number
77757
Product Number
2
Dosage Form
-
Strength
100MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
LAMOTRIGINE
Product Number
3
Dosage Form
-
Strength
150MG
Approval Date
-
Active Ingredient
LAMOTRIGINE
Application Number
77757
Product Number
3
Dosage Form
-
Strength
150MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
LAMOTRIGINE
Product Number
4
Dosage Form
-
Strength
200MG
Approval Date
-
Active Ingredient
LAMOTRIGINE
Application Number
77757
Product Number
4
Dosage Form
-
Strength
200MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
MODAFINIL
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
-
Active Ingredient
MODAFINIL
Application Number
77892
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
MODAFINIL
Product Number
2
Dosage Form
-
Strength
200MG
Approval Date
-
Active Ingredient
MODAFINIL
Application Number
77892
Product Number
2
Dosage Form
-
Strength
200MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
WYGESIC
Product Number
1
Dosage Form
-
Strength
650MG;65MG
Approval Date
1982-01-01
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE HYDROCHLORIDE
Application Number
84999
Product Number
1
Dosage Form
-
Strength
650MG;65MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Status Breakdown
17 total- Unclassified
- Discontinued
Official Source
FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.
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Drug Name
ESCITALOPRAM OXALATE
Application Number
78219
Product Number
1
Active Ingredient
ESCITALOPRAM OXALATE
Dosage Form
-
Strength
5MG
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