01 3ACARBOSE
02 3ACETYLCYSTEINE
03 5ATROPINE SULFATE
04 1AZELASTINE HYDROCHLORIDE
05 1BEPOTASTINE BESILATE
06 1BIMATOPROST
07 2BRIMONIDINE TARTRATE
08 1BRIMONIDINE TARTRATE; TIMOLOL MALEATE
09 2BUPIVACAINE HYDROCHLORIDE
10 1BUPRENORPHINE HYDROCHLORIDE
11 1CABERGOLINE
12 1CALCIUM CHLORIDE
13 2CALCIUM GLUCONATE
14 3CISATRACURIUM BESYLATE
15 1CLONIDINE HYDROCHLORIDE
16 1CUPRIC CHLORIDE
17 2CYANOCOBALAMIN
18 3DEXAMETHASONE SODIUM PHOSPHATE
19 2DEXMEDETOMIDINE HYDROCHLORIDE
20 2DICYCLOMINE HYDROCHLORIDE
21 1DORZOLAMIDE HYDROCHLORIDE
22 1DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE
23 4DOXYCYCLINE
24 3DROXIDOPA
25 1EPINASTINE HYDROCHLORIDE
26 1GLYCOPYRROLATE
27 2HALOPERIDOL DECANOATE
28 1ISOPROTERENOL HYDROCHLORIDE
29 1ISOSULFAN BLUE
30 1LACOSAMIDE
31 1LATANOPROST
32 1METHOCARBAMOL
33 1MOXIFLOXACIN HYDROCHLORIDE
34 4NALBUPHINE HYDROCHLORIDE
35 2NALOXONE HYDROCHLORIDE
36 2OFLOXACIN
37 2OLOPATADINE HYDROCHLORIDE
38 1PHENYLEPHRINE HYDROCHLORIDE
39 3PILOCARPINE HYDROCHLORIDE
40 1POLYMYXIN B SULFATE; TRIMETHOPRIM SULFATE
41 2POTASSIUM PHOSPHATE, DIBASIC; POTASSIUM PHOSPHATE, MONOBASIC
42 1PROCHLORPERAZINE EDISYLATE
43 1PROPARACAINE HYDROCHLORIDE
44 7ROPIVACAINE HYDROCHLORIDE
45 6SELEGILINE
46 1SODIUM NITROPRUSSIDE
47 1SUCCINYLCHOLINE CHLORIDE
48 1SULFAMETHOXAZOLE; TRIMETHOPRIM
49 1TETRACAINE HYDROCHLORIDE
50 1TIMOLOL
51 5TIMOLOL MALEATE
52 2TIZANIDINE HYDROCHLORIDE
53 1TOBRAMYCIN
54 1TRAVOPROST
55 1TROPICAMIDE
56 1VALGANCICLOVIR HYDROCHLORIDE
57 4VERAPAMIL HYDROCHLORIDE
58 1ZINC CHLORIDE
59 2ZINC SULFATE
60 2ZOLMITRIPTAN
01 29SOMERSET
02 85SOMERSET THERAPS LLC
01 5CAPSULE;ORAL
02 3FILM, EXTENDED RELEASE;TRANSDERMAL
03 26INJECTABLE;INJECTION
04 1INJECTABLE;INTRAVENOUS
05 2SOLUTION, GEL FORMING/DROPS;OPHTHALMIC
06 25SOLUTION/DROPS;OPHTHALMIC
07 1SOLUTION/DROPS;OTIC
08 1SOLUTION;IM-IV
09 2SOLUTION;INHALATION, ORAL
10 7SOLUTION;INJECTION
11 4SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
12 16SOLUTION;INTRAVENOUS
13 1SOLUTION;INTRAVENOUS, INTRAMUSCULAR, SUBCUTANEOUS, INTRAOSSEOUS, ENDOT
14 4SOLUTION;OPHTHALMIC
15 1SOLUTION;SUBCUTANEOUS
16 3SYSTEM; TRANSDERMAL
17 1TABLET, EXTENDED RELEASE;ORAL
18 11TABLET;ORAL
01 10.004%
02 10.005%
03 10.03%
04 20.05%
05 10.1%
06 10.1MG
07 10.2%
08 10.2%;EQ 0.5% BASE
09 10.25%
10 20.2MG/ML
11 30.3%
12 20.4MG/ML
13 10.4MG/ML (0.4MG/ML)
14 40.5%
15 10.5MG
16 10.5MG/5ML (0.1MG/ML)
17 41%
18 11.18GM/5ML (236MG/ML);1.12GM/5ML (224MG/ML)
19 11.5%
20 110%
21 110,000 UNITS/ML;EQ 1MG BASE/ML
22 2100MG
23 2100MG/10ML (10MG/ML)
24 1100MG/20ML (5MG/ML)
25 1100MG/ML
26 110GM/100ML (100MG/ML)
27 210MG/4ML (2.5MG/ML)
28 210MG/ML
29 110MG/ML (10MG/ML)
30 112MG
31 112MG/24HR
32 1150MG/20ML (7.5MG/ML)
33 1150MG/30ML (5MG/ML)
34 11GM/10ML (100MG/ML)
35 21MG/ML
36 11MG/ML (1MG/ML)
37 12%
38 12.5MG
39 120%
40 1200MG
41 1200MG/10ML (20MG/ML)
42 2200MG/20ML (10MG/ML)
43 120MG/10ML (2MG/ML)
44 120MG/ML
45 120MG/ML (20MG/ML)
46 125MG
47 125MG/ML
48 13.54GM/15ML (236MG/ML);3.36GM/15ML (224MG/ML)
49 1300MG
50 14%
51 140MG/20ML (2MG/ML)
52 150MG
53 150MG/5ML (10MG/ML)
54 15GM/50ML (100MG/ML)
55 15MG
56 25MG/2ML (2.5MG/ML)
57 16GM/30ML (200MG/ML)
58 16MG
59 16MG/24HR
60 180MG/ML;16MG/ML
61 18MG/20ML (0.4MG/ML)
62 19MG
63 19MG/24HR
64 1EQ 0.1% BASE
65 1EQ 0.2% BASE
66 2EQ 0.25% BASE
67 1EQ 0.3MG BASE/ML
68 1EQ 0.4MG COPPER/ML
69 4EQ 0.5% BASE
70 1EQ 100MG BASE
71 1EQ 100MG BASE/ML
72 1EQ 10MG BASE/ML
73 2EQ 10MG PHOSPHATE/ML
74 1EQ 150MG BASE
75 1EQ 1MG BASE/10ML (EQ 100MCG BASE/ML)
76 1EQ 1MG ZINC/ML
77 1EQ 2% BASE
78 1EQ 2% BASE;EQ 0.5% BASE
79 1EQ 25MG BASE/5ML (EQ 5MG BASE/ML)
80 2EQ 2MG BASE/ML
81 1EQ 30MG BASE/10ML (EQ 3MG BASE/ML)
82 1EQ 400MCG BASE/4ML (EQ 100MCG BASE/ML)
83 1EQ 450MG BASE
84 1EQ 4MG BASE
85 1EQ 4MG PHOSPHATE/ML
86 1EQ 50MG BASE
87 1EQ 50MG BASE/ML
88 1EQ 5MG BASE/ML
89 1EQ 6MG BASE
90 1EQ 75MG BASE
01 114USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ACARBOSE
Dosage Strength : 25MG
Packaging :
Approval Date : 2013-10-17
Application Number : 91343
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ACARBOSE
Dosage Strength : 50MG
Packaging :
Approval Date : 2013-10-17
Application Number : 91343
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ACARBOSE
Dosage Strength : 100MG
Packaging :
Approval Date : 2013-10-17
Application Number : 91343
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INTRAVENOUS
Brand Name : ACETYLCYSTEINE
Dosage Strength : 6GM/30ML (200MG/ML)
Packaging :
Approval Date : 2024-06-07
Application Number : 218397
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;INHALATION, ORA...
Brand Name : ACETYLCYSTEINE
Dosage Strength : 10%
Packaging :
Approval Date : 2025-02-12
Application Number : 219194
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;INHALATION, ORA...
Brand Name : ACETYLCYSTEINE
Dosage Strength : 20%
Packaging :
Approval Date : 2025-02-12
Application Number : 219194
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION/DROPS;OPHTHALMI...
Brand Name : ATROPINE SULFATE
Dosage Strength : 1%
Packaging :
Approval Date : 2024-07-01
Application Number : 215618
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;INTRAVENOUS
Brand Name : ATROPINE SULFATE
Dosage Strength : 0.4MG/ML (0.4MG/ML)
Packaging :
Approval Date : 2024-07-03
Application Number : 215969
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;INTRAVENOUS
Brand Name : ATROPINE SULFATE
Dosage Strength : 1MG/ML (1MG/ML)
Packaging :
Approval Date : 2024-07-03
Application Number : 215969
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION/DROPS;OPHTHALMI...
Brand Name : ATROPINE SULFATE
Dosage Strength : 1%
Packaging :
Approval Date : 2024-04-29
Application Number : 217791
Regulatory Info : RX
Registration Country : USA
