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NDC properties for "Altacaine 0.5 % Ophthalmic Solution" (RxCUI 1547773)

About this data

The tables show NDC propoerties for Altacaine 0.5 % Ophthalmic Solution with the RxCUI 1547773

This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product

Details for Altacaine 0.5 % Ophthalmic Solution (RxCUI 1547773)

MMSL_CODEBD3004
RxCUI1547773
Prescribable SynonymALTACAINE 0.5 % Ophthalmic Solution
RXNAV_STRAltacaine 0.5 % Ophthalmic Solution
RxNorm Nametetracaine hydrochloride 5 MG/ML Ophthalmic Solution [Altacaine]
RxNorm SynonymAltacaine 0.5 % Ophthalmic Solution
Related queriesInteractions (for RxCUI 1547773)



NDC Properties

NDC Item 59390018107

NDC 959390-181
NDC 1059390-181-07
NDC Item59390018107
FDA SPL set id443832
LabelerAltaire Pharmaceuticals Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryUNAPPROVED DRUG OTHER
Marketing effective time high2019-07-15
Marketing effective time low2002-02-01
Marketing statusCOMPLETED
UNAPPROVED_DRUG_OTHERN/A
Related queriesProperties for NDC 9 59390-181

NDC Item 59390018113

NDC 959390-181
NDC 1059390-181-13
NDC Item59390018113
Packaging15 mL in 1 BOTTLE, DROPPER (59390-181-13)
FDA SPL set id443832
LabelerAltaire Pharmaceuticals Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryUNAPPROVED DRUG OTHER
Marketing effective time high2019-07-15
Marketing effective time low2002-02-01
Marketing statusCOMPLETED
UNAPPROVED_DRUG_OTHERN/A
Related queriesProperties for NDC 9 59390-181

NDC Item 59390018118

NDC 959390-181
NDC 1059390-181-18
NDC Item59390018118
FDA SPL set id443832
LabelerAltaire Pharmaceuticals Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryUNAPPROVED DRUG OTHER
Marketing effective time high2019-07-15
Marketing effective time low2002-02-01
Marketing statusCOMPLETED
UNAPPROVED_DRUG_OTHERN/A
Related queriesProperties for NDC 9 59390-181

NDC Item 59390018107

NDC 959390-181
NDC 1059390-181-07
NDC Item59390018107
FDA SPL set id443832
LabelerAltaire Pharmaceuticals Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryUNAPPROVED DRUG OTHER
Marketing effective time high2019-07-15
Marketing effective time low2002-02-01
Marketing statusCOMPLETED
UNAPPROVED_DRUG_OTHERN/A
Related queriesProperties for NDC 9 59390-181

NDC Item 59390018113

NDC 959390-181
NDC 1059390-181-13
NDC Item59390018113
Packaging15 mL in 1 BOTTLE, DROPPER (59390-181-13)
FDA SPL set id443832
LabelerAltaire Pharmaceuticals Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryUNAPPROVED DRUG OTHER
Marketing effective time high2019-07-15
Marketing effective time low2002-02-01
Marketing statusCOMPLETED
UNAPPROVED_DRUG_OTHERN/A
Related queriesProperties for NDC 9 59390-181

NDC Item 59390018118

NDC 959390-181
NDC 1059390-181-18
NDC Item59390018118
FDA SPL set id443832
LabelerAltaire Pharmaceuticals Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryUNAPPROVED DRUG OTHER
Marketing effective time high2019-07-15
Marketing effective time low2002-02-01
Marketing statusCOMPLETED
UNAPPROVED_DRUG_OTHERN/A
Related queriesProperties for NDC 9 59390-181

NDC Item 59390018107

NDC 959390-181
NDC 1059390-181-07
NDC Item59390018107
FDA SPL set id443832
LabelerAltaire Pharmaceuticals Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryUNAPPROVED DRUG OTHER
Marketing effective time high2019-07-15
Marketing effective time low2002-02-01
Marketing statusCOMPLETED
UNAPPROVED_DRUG_OTHERN/A
Related queriesProperties for NDC 9 59390-181

NDC Item 59390018113

NDC 959390-181
NDC 1059390-181-13
NDC Item59390018113
Packaging15 mL in 1 BOTTLE, DROPPER (59390-181-13)
FDA SPL set id443832
LabelerAltaire Pharmaceuticals Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryUNAPPROVED DRUG OTHER
Marketing effective time high2019-07-15
Marketing effective time low2002-02-01
Marketing statusCOMPLETED
UNAPPROVED_DRUG_OTHERN/A
Related queriesProperties for NDC 9 59390-181

NDC Item 59390018118

NDC 959390-181
NDC 1059390-181-18
NDC Item59390018118
FDA SPL set id443832
LabelerAltaire Pharmaceuticals Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryUNAPPROVED DRUG OTHER
Marketing effective time high2019-07-15
Marketing effective time low2002-02-01
Marketing statusCOMPLETED
UNAPPROVED_DRUG_OTHERN/A
Related queriesProperties for NDC 9 59390-181