Par Pharmaceutical Unclassified
FDA Approved Drugs
Par Pharmaceutical Unclassified
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 23
- Latest Approval Date -
- Data Source FDA
- First Approval Date -
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Par Pharmaceutical Unclassified
300 Tice BoulevardWoodcliff Lake, NJ 07677
U.S.A
www.parpharm.com/ View on MapFDA Approved Drug Records ( 23 records )
Drug Name
CITRIC ACID; MAGNESIUM OXIDE; SODIUM PICOSULFATE
Product Number
1
Dosage Form
-
Strength
12GM/PACKET;3.5GM/PACKET;10MG/PACKET
Approval Date
-
Active Ingredient
CITRIC ACID; MAGNESIUM OXIDE; SODIUM PICOSULFATE
Application Number
205743
Product Number
1
Dosage Form
-
Strength
12GM/PACKET;3.5GM/PACKET;10MG/PACKET
Approval Date
-
Regulatory Status
Unclassified
Drug Name
CYCLOBENZAPRINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
15MG
Approval Date
-
Active Ingredient
CYCLOBENZAPRINE HYDROCHLORIDE
Application Number
90864
Product Number
1
Dosage Form
-
Strength
15MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
CYCLOBENZAPRINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
30MG
Approval Date
-
Active Ingredient
CYCLOBENZAPRINE HYDROCHLORIDE
Application Number
90864
Product Number
2
Dosage Form
-
Strength
30MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
DEXTROMETHORPHAN HYDROBROMIDE AND QUINIDINE SULFATE
Product Number
1
Dosage Form
-
Strength
20MG;10MG
Approval Date
-
Active Ingredient
DEXTROMETHORPHAN HYDROBROMIDE;QUINIDINE SULFATE
Application Number
202993
Product Number
1
Dosage Form
-
Strength
20MG;10MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
DONEPEZIL HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
-
Active Ingredient
DONEPEZIL HYDROCHLORIDE
Application Number
76893
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
DONEPEZIL HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
-
Active Ingredient
DONEPEZIL HYDROCHLORIDE
Application Number
76893
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
DOXEPIN HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 25MG BASE
Approval Date
-
Active Ingredient
DOXEPIN HYDROCHLORIDE
Application Number
71437
Product Number
1
Dosage Form
-
Strength
EQ 25MG BASE
Approval Date
-
Regulatory Status
Unclassified
Drug Name
FINGOLIMOD
Product Number
1
Dosage Form
-
Strength
0.5MG
Approval Date
-
Active Ingredient
FINGOLIMOD
Application Number
207965
Product Number
1
Dosage Form
-
Strength
0.5MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
FLUVASTATIN SODIUM
Product Number
1
Dosage Form
-
Strength
80MG
Approval Date
-
Active Ingredient
FLUVASTATIN SODIUM
Application Number
78872
Product Number
1
Dosage Form
-
Strength
80MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
LATANOPROST
Product Number
1
Dosage Form
-
Strength
0.005%
Approval Date
-
Active Ingredient
LATANOPROST
Application Number
76218
Product Number
1
Dosage Form
-
Strength
0.005%
Approval Date
-
Regulatory Status
Unclassified
Drug Name
LURASIDONE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
20MG
Approval Date
-
Active Ingredient
LURASIDONE HYDROCHLORIDE
Application Number
207948
Product Number
1
Dosage Form
-
Strength
20MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
LURASIDONE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
40MG
Approval Date
-
Active Ingredient
LURASIDONE HYDROCHLORIDE
Application Number
207948
Product Number
2
Dosage Form
-
Strength
40MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
LURASIDONE HYDROCHLORIDE
Product Number
3
Dosage Form
-
Strength
60MG
Approval Date
-
Active Ingredient
LURASIDONE HYDROCHLORIDE
Application Number
207948
Product Number
3
Dosage Form
-
Strength
60MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
LURASIDONE HYDROCHLORIDE
Product Number
4
Dosage Form
-
Strength
80MG
Approval Date
-
Active Ingredient
LURASIDONE HYDROCHLORIDE
Application Number
207948
Product Number
4
Dosage Form
-
Strength
80MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
LURASIDONE HYDROCHLORIDE
Product Number
5
Dosage Form
-
Strength
120MG
Approval Date
-
Active Ingredient
LURASIDONE HYDROCHLORIDE
Application Number
207948
Product Number
5
Dosage Form
-
Strength
120MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
MILNACIPRAN HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
12.5MG
Approval Date
-
Active Ingredient
MILNACIPRAN HYDROCHLORIDE
Application Number
205062
Product Number
1
Dosage Form
-
Strength
12.5MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
MILNACIPRAN HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
25MG
Approval Date
-
Active Ingredient
MILNACIPRAN HYDROCHLORIDE
Application Number
205062
Product Number
2
Dosage Form
-
Strength
25MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
MILNACIPRAN HYDROCHLORIDE
Product Number
3
Dosage Form
-
Strength
50MG
Approval Date
-
Active Ingredient
MILNACIPRAN HYDROCHLORIDE
Application Number
205062
Product Number
3
Dosage Form
-
Strength
50MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
MILNACIPRAN HYDROCHLORIDE
Product Number
4
Dosage Form
-
Strength
100MG
Approval Date
-
Active Ingredient
MILNACIPRAN HYDROCHLORIDE
Application Number
205062
Product Number
4
Dosage Form
-
Strength
100MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
SAXAGLIPTIN
Product Number
2
Dosage Form
-
Strength
5MG
Approval Date
-
Active Ingredient
SAXAGLIPTIN
Application Number
205959
Product Number
2
Dosage Form
-
Strength
5MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
SUMATRIPTAN; NAPROXEN SODIUM
Product Number
1
Dosage Form
-
Strength
85MG; 500MG
Approval Date
-
Active Ingredient
SUMATRIPTAN; NAPROXEN SODIUM
Application Number
90753
Product Number
1
Dosage Form
-
Strength
85MG; 500MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
TRAVOPROST
Product Number
1
Dosage Form
-
Strength
0.004%
Approval Date
-
Active Ingredient
TRAVOPROST
Application Number
91341
Product Number
1
Dosage Form
-
Strength
0.004%
Approval Date
-
Regulatory Status
Unclassified
Drug Name
VARDENAFIL HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
-
Active Ingredient
VARDENAFIL HYDROCHLORIDE
Application Number
204786
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
-
Regulatory Status
Unclassified
Drug Status Breakdown
23 total- Unclassified
Official Source
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Drug Name
CITRIC ACID; MAGNESIUM OXIDE; SODIUM PICOSULFATE
Application Number
205743
Product Number
1
Active Ingredient
CITRIC ACID; MAGNESIUM OXIDE; SODIUM PICOSULFATE
Dosage Form
-
Strength
12GM/PACKET;3.5GM/PACKET;10MG/PACKET
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