01 2ALBUTEROL SULFATE
02 1CROMOLYN SODIUM
03 2DIAZEPAM
04 1LEVORPHANOL TARTRATE
05 6PHENDIMETRAZINE TARTRATE
06 6PROGESTERONE
01 2CAPSULE, EXTENDED RELEASE;ORAL
02 3CAPSULE; ORAL
03 4CAPSULE;ORAL
04 1SOLUTION;INHALATION
05 8TABLET;ORAL
01 2100MG
02 2105MG
03 110MG/ML
04 2200MG
05 22MG
06 2300MG
07 435MG
08 15MG
09 1EQ 2MG BASE
10 1EQ 4MG BASE
01 7DISCN
02 8RX
03 3Blank
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ALBUTEROL SULFATE
Dosage Strength : EQ 2MG BASE
Approval Date : 2018-10-26
Application Number : 211397
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ALBUTEROL SULFATE
Dosage Strength : EQ 4MG BASE
Approval Date : 2018-10-26
Application Number : 211397
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AN
Dosage Form : SOLUTION; INHALATION
Proprietary Name : CROMOLYN SODIUM
Dosage Strength : 10MG/ML
Approval Date : 2000-04-21
Application Number : 75437
RX/OTC/DISCN : RX
RLD : No
TE Code : AN
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : DIAZEPAM
Dosage Strength : 2MG
Approval Date : 1986-02-25
Application Number : 70462
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : DIAZEPAM
Dosage Strength : 5MG
Approval Date : 1986-02-25
Application Number : 70463
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : LEVORPHANOL TARTRATE
Dosage Strength : 2MG
Approval Date : 2018-12-13
Application Number : 211484
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : PHENDIMETRAZINE TARTRATE
Dosage Strength : 35MG
Approval Date : 1982-01-01
Application Number : 85497
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code : AA
Dosage Form : TABLET; ORAL
Proprietary Name : PHENDIMETRAZINE TARTRATE
Dosage Strength : 35MG
Approval Date : 1982-01-01
Application Number : 85588
RX/OTC/DISCN : RX
RLD : No
TE Code : AA
RLD : No
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : PHENDIMETRAZINE TARTRATE
Dosage Strength : 35MG
Approval Date : 1982-01-01
Application Number : 85695
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : PHENDIMETRAZINE TARTRATE
Dosage Strength : 35MG
Approval Date : 1982-01-01
Application Number : 86365
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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