01 1ASPIRIN; BUTALBITAL
02 1BENTIROMIDE
03 3BETAMETHASONE DIPROPIONATE
04 3BETAMETHASONE VALERATE
05 1CYANOCOBALAMIN
06 2DYPHYLLINE
07 1ESTRADIOL VALERATE; TESTOSTERONE ENANTHATE
08 4FLUOCINOLONE ACETONIDE
09 1GENTIAN VIOLET
10 2METRONIDAZOLE
11 2NEOMYCIN SULFATE; TRIAMCINOLONE ACETONIDE
12 1NYSTATIN
13 2NYSTATIN; TRIAMCINOLONE ACETONIDE
14 4POTASSIUM CHLORIDE
15 5TRIAMCINOLONE ACETONIDE
16 1TRIPLE SULFA (SULFABENZAMIDE;SULFACETAMIDE;SULFATHIAZOLE)
17 1XYLOSE
01 2CAPSULE, EXTENDED RELEASE;ORAL
02 9CREAM;TOPICAL
03 1CREAM;VAGINAL
04 2INJECTABLE;INJECTION
05 2LOTION;TOPICAL
06 7OINTMENT;TOPICAL
07 1POWDER;ORAL
08 1SOLUTION;ORAL
09 1SOLUTION;TOPICAL
10 1SUPPOSITORY;VAGINAL
11 1SUSPENSION;ORAL
12 2TABLET, EXTENDED RELEASE;ORAL
13 5TABLET;ORAL
01 20.01%
02 40.025%
03 20.1%
04 10.4%
05 10.5%
06 2100,000 UNITS/GM;0.1%
07 1100,000 UNITS/ML
08 210MEQ
09 11MG/ML
10 1200MG
11 1250MG
12 125GM/BOT
13 13.7%;2.86%;3.42%
14 1400MG
15 1500MG
16 1500MG/7.5ML
17 16.7MEQ
18 1650MG;50MG
19 18MEQ
20 18MG/ML;180MG/ML
21 3EQ 0.05% BASE
22 3EQ 0.1% BASE
23 2EQ 3.5MG BASE/GM;0.1%
01 35DISCN
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : AXOTAL
Dosage Strength : 650MG;50MG
Approval Date : 1983-10-13
Application Number : 88305
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : SOLUTION; ORAL
Proprietary Name : CHYMEX
Dosage Strength : 500MG/7.5ML
Approval Date : 1983-12-29
Application Number : 18366
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : CREAM; TOPICAL
Proprietary Name : ALPHATREX
Dosage Strength : EQ 0.05% BASE
Approval Date : 1984-06-26
Application Number : 19138
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : OINTMENT; TOPICAL
Proprietary Name : ALPHATREX
Dosage Strength : EQ 0.05% BASE
Approval Date : 1984-09-04
Application Number : 19143
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : LOTION; TOPICAL
Proprietary Name : ALPHATREX
Dosage Strength : EQ 0.05% BASE
Approval Date : 1985-08-12
Application Number : 70273
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : CREAM; TOPICAL
Proprietary Name : BETATREX
Dosage Strength : EQ 0.1% BASE
Approval Date : 1983-08-31
Application Number : 18862
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : OINTMENT; TOPICAL
Proprietary Name : BETATREX
Dosage Strength : EQ 0.1% BASE
Approval Date : 1983-08-31
Application Number : 18863
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : LOTION; TOPICAL
Proprietary Name : BETATREX
Dosage Strength : EQ 0.1% BASE
Approval Date : 1983-08-31
Application Number : 18867
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : RUVITE
Dosage Strength : 1MG/ML
Approval Date : 1982-01-01
Application Number : 80570
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : DILOR
Dosage Strength : 200MG
Approval Date : 1982-01-01
Application Number : 84514
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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