Amneal Pharmaceuticals Discontinued
FDA Approved Drugs
Amneal Pharmaceuticals Discontinued
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 21
- Latest Approval Date Mar 27, 2024
- Data Source FDA
- First Approval Date Sep 02, 2008
Company Overview
Company
Amneal Pharmaceuticals Discontinued
Country
U.S.A
Website
Social Profiles
Company Snapshot
Amneal Pharmaceuticals Discontinued
400 Crossing Boulevard, 3rd Floor Bridgewater, New Jersey 08807
U.S.A
amneal.com/ nfo@rakspharma.com View on MapFDA Approved Drug Records ( 21 records )
Drug Name
CALCIUM ACETATE
Product Number
1
Dosage Form
-
Strength
667MG
Approval Date
2014-10-06
Active Ingredient
CALCIUM ACETATE
Application Number
201658
Product Number
1
Dosage Form
-
Strength
667MG
Approval Date
2014-10-06
Regulatory Status
Discontinued
Drug Name
CAPECITABINE
Product Number
1
Dosage Form
-
Strength
150MG
Approval Date
2017-02-28
Active Ingredient
CAPECITABINE
Application Number
204741
Product Number
1
Dosage Form
-
Strength
150MG
Approval Date
2017-02-28
Regulatory Status
Discontinued
Drug Name
CAPECITABINE
Product Number
2
Dosage Form
-
Strength
500MG
Approval Date
2017-02-28
Active Ingredient
CAPECITABINE
Application Number
204741
Product Number
2
Dosage Form
-
Strength
500MG
Approval Date
2017-02-28
Regulatory Status
Discontinued
Drug Name
CLINDAMYCIN PALMITATE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 75MG BASE/5ML
Approval Date
2014-03-13
Active Ingredient
CLINDAMYCIN PALMITATE HYDROCHLORIDE
Application Number
203513
Product Number
1
Dosage Form
-
Strength
EQ 75MG BASE/5ML
Approval Date
2014-03-13
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
300MG;10MG
Approval Date
2016-11-29
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Application Number
207137
Product Number
1
Dosage Form
-
Strength
300MG;10MG
Approval Date
2016-11-29
Regulatory Status
Discontinued
Drug Name
LACOSAMIDE
Product Number
1
Dosage Form
-
Strength
10MG/ML
Approval Date
2024-03-27
Active Ingredient
LACOSAMIDE
Application Number
204839
Product Number
1
Dosage Form
-
Strength
10MG/ML
Approval Date
2024-03-27
Regulatory Status
Discontinued
Drug Name
LINEZOLID
Product Number
1
Dosage Form
-
Strength
600MG
Approval Date
2015-12-21
Active Ingredient
LINEZOLID
Application Number
204536
Product Number
1
Dosage Form
-
Strength
600MG
Approval Date
2015-12-21
Regulatory Status
Discontinued
Drug Name
LORAZEPAM
Product Number
1
Dosage Form
-
Strength
0.5MG
Approval Date
2010-06-23
Active Ingredient
LORAZEPAM
Application Number
78826
Product Number
1
Dosage Form
-
Strength
0.5MG
Approval Date
2010-06-23
Regulatory Status
Discontinued
Drug Name
LORAZEPAM
Product Number
2
Dosage Form
-
Strength
1MG
Approval Date
2010-06-23
Active Ingredient
LORAZEPAM
Application Number
78826
Product Number
2
Dosage Form
-
Strength
1MG
Approval Date
2010-06-23
Regulatory Status
Discontinued
Drug Name
LORAZEPAM
Product Number
3
Dosage Form
-
Strength
2MG
Approval Date
2010-06-23
Active Ingredient
LORAZEPAM
Application Number
78826
Product Number
3
Dosage Form
-
Strength
2MG
Approval Date
2010-06-23
Regulatory Status
Discontinued
Drug Name
NITROFURANTOIN
Product Number
1
Dosage Form
-
Strength
25MG/5ML
Approval Date
2011-05-11
Active Ingredient
NITROFURANTOIN
Application Number
201679
Product Number
1
Dosage Form
-
Strength
25MG/5ML
Approval Date
2011-05-11
Regulatory Status
Discontinued
Drug Name
NITROFURANTOIN (MONOHYDRATE/MACROCRYSTALS)
Product Number
1
Dosage Form
-
Strength
75MG;25MG
Approval Date
2017-05-15
Active Ingredient
NITROFURANTOIN; NITROFURANTOIN, MACROCRYSTALLINE
Application Number
207372
Product Number
1
Dosage Form
-
Strength
75MG;25MG
Approval Date
2017-05-15
Regulatory Status
Discontinued
Drug Name
NIZATIDINE
Product Number
1
Dosage Form
-
Strength
15MG/ML
Approval Date
2009-11-18
Active Ingredient
NIZATIDINE
Application Number
90576
Product Number
1
Dosage Form
-
Strength
15MG/ML
Approval Date
2009-11-18
Regulatory Status
Discontinued
Drug Name
PREDNISOLONE SODIUM PHOSPHATE
Product Number
1
Dosage Form
-
Strength
EQ 15MG BASE/5ML
Approval Date
2009-03-10
Active Ingredient
PREDNISOLONE SODIUM PHOSPHATE
Application Number
78345
Product Number
1
Dosage Form
-
Strength
EQ 15MG BASE/5ML
Approval Date
2009-03-10
Regulatory Status
Discontinued
Drug Name
PROMETHAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
6.25MG/5ML
Approval Date
2009-12-30
Active Ingredient
PROMETHAZINE HYDROCHLORIDE
Application Number
40882
Product Number
1
Dosage Form
-
Strength
6.25MG/5ML
Approval Date
2009-12-30
Regulatory Status
Discontinued
Drug Name
RANITIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 15MG BASE/ML
Approval Date
2008-09-02
Active Ingredient
RANITIDINE HYDROCHLORIDE
Application Number
78312
Product Number
1
Dosage Form
-
Strength
EQ 15MG BASE/ML
Approval Date
2008-09-02
Regulatory Status
Discontinued
Drug Name
VENLAFAXINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 25MG BASE
Approval Date
2010-05-11
Active Ingredient
VENLAFAXINE HYDROCHLORIDE
Application Number
79098
Product Number
1
Dosage Form
-
Strength
EQ 25MG BASE
Approval Date
2010-05-11
Regulatory Status
Discontinued
Drug Name
VENLAFAXINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
EQ 37.5MG BASE
Approval Date
2010-05-11
Active Ingredient
VENLAFAXINE HYDROCHLORIDE
Application Number
79098
Product Number
2
Dosage Form
-
Strength
EQ 37.5MG BASE
Approval Date
2010-05-11
Regulatory Status
Discontinued
Drug Name
VENLAFAXINE HYDROCHLORIDE
Product Number
3
Dosage Form
-
Strength
EQ 50MG BASE
Approval Date
2010-05-11
Active Ingredient
VENLAFAXINE HYDROCHLORIDE
Application Number
79098
Product Number
3
Dosage Form
-
Strength
EQ 50MG BASE
Approval Date
2010-05-11
Regulatory Status
Discontinued
Drug Name
VENLAFAXINE HYDROCHLORIDE
Product Number
4
Dosage Form
-
Strength
EQ 75MG BASE
Approval Date
2010-05-11
Active Ingredient
VENLAFAXINE HYDROCHLORIDE
Application Number
79098
Product Number
4
Dosage Form
-
Strength
EQ 75MG BASE
Approval Date
2010-05-11
Regulatory Status
Discontinued
Drug Name
VENLAFAXINE HYDROCHLORIDE
Product Number
5
Dosage Form
-
Strength
EQ 100MG BASE
Approval Date
2010-05-11
Active Ingredient
VENLAFAXINE HYDROCHLORIDE
Application Number
79098
Product Number
5
Dosage Form
-
Strength
EQ 100MG BASE
Approval Date
2010-05-11
Regulatory Status
Discontinued
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Drug Status Breakdown
21 total- 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
CALCIUM ACETATE
Application Number
201658
Product Number
1
Active Ingredient
CALCIUM ACETATE
Dosage Form
-
Strength
667MG
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