01 1ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
02 5ETODOLAC
03 1KETOTIFEN FUMARATE
04 2METHSCOPOLAMINE BROMIDE
05 3METOLAZONE
06 1ORPHENADRINE CITRATE
07 2PINDOLOL
08 1PRIMAQUINE PHOSPHATE
01 16BAYSHORE PHARMS LLC
01 1SOLUTION/DROPS;OPHTHALMIC
02 4TABLET, EXTENDED RELEASE;ORAL
03 11TABLET;ORAL
01 10.025MG;2.5MG
02 1100MG
03 210MG
04 22.5MG
05 2400MG
06 2500MG
07 35MG
08 1600MG
09 1EQ 0.025% BASE
10 1EQ 15MG BASE
01 16USA
Regulatory Info : RX
Registration Country : USA
ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Brand Name : DIPHENOXYLATE HYDROCHLORI...
Dosage Strength : 0.025MG;2.5MG
Packaging :
Approval Date : 2018-11-13
Application Number : 210819
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ETODOLAC
Dosage Strength : 400MG
Packaging :
Approval Date : 2020-12-16
Application Number : 210704
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ETODOLAC
Dosage Strength : 500MG
Packaging :
Approval Date : 2020-12-16
Application Number : 210704
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET, EXTENDED RELEASE...
Brand Name : ETODOLAC
Dosage Strength : 400MG
Packaging :
Approval Date : 2020-11-24
Application Number : 212263
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET, EXTENDED RELEASE...
Brand Name : ETODOLAC
Dosage Strength : 500MG
Packaging :
Approval Date : 2020-11-24
Application Number : 212263
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET, EXTENDED RELEASE...
Brand Name : ETODOLAC
Dosage Strength : 600MG
Packaging :
Approval Date : 2020-11-24
Application Number : 212263
Regulatory Info : RX
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Dosage Form : SOLUTION/DROPS;OPHTHALMI...
Brand Name : KETOTIFEN FUMARATE
Dosage Strength : EQ 0.025% BASE
Packaging :
Approval Date : 2020-06-01
Application Number : 204059
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : METHSCOPOLAMINE BROMIDE
Dosage Strength : 2.5MG
Packaging :
Approval Date : 2012-09-24
Application Number : 200602
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : METHSCOPOLAMINE BROMIDE
Dosage Strength : 5MG
Packaging :
Approval Date : 2012-09-24
Application Number : 200602
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : METOLAZONE
Dosage Strength : 5MG
Packaging :
Approval Date : 2021-03-30
Application Number : 214799
Regulatory Info : RX
Registration Country : USA
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