atropine sulfate

Product NDC
0065-0817
11-digit product format
000650817
Labeler code
0065
Product ID
0065-0817_96e742ed-f4e5-4e9c-b383-7c8b9fac1a43
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
atropine sulfate
Dosage form
SOLUTION
Route
OPHTHALMIC
Labeler
Alcon Laboratories, Inc.
Application
NDA208151
Marketing category
NDA
Marketing start
2022-11-01
Substance
ATROPINE SULFATE
Active strength
10 mg/mL
Pharmacologic classes
Anticholinergic [EPC], Cholinergic Antagonists [MoA], Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
atropine sulfate
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ATROPINE SULFATE10 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii03J5ZE7KA5
Rxcui1190655

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c78bd43-efb4-4aeb-b7d8-eff1532f7822Product name420250801
41231c1e-8789-4da7-ac52-77fa90a85bf5Product name220250304
e77ab9a2-80cf-4832-bff0-469bbc7cbcd0Product name220250214
5f84b7a7-523a-f042-dffb-1dadcd9b2407Product name420240110
0cbc6fb2-78c0-4b88-98f0-a4cc76ff95caProduct name120230719
04cd5dc0-102f-46cb-8dbc-ca38dd2628d0Product name320230317
dfd25202-b8d2-4628-9213-f3e0f9eafce5Product name420210513
4199bf9b-4718-828a-6dd6-ac2fbbd61687Product name120140508
4edd8af5-cea7-ae42-8023-e91c5335db1dProduct name120140508
d3908afb-7784-440f-c406-88294732d36aProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0065-0817-01atropine sulfate1 in 1 CARTONSOLUTION18
0065-0817-01atropine sulfate5 mL in 1 BOTTLE, DROPPERSOLUTION58
0065-0817-02atropine sulfate2 mL in 1 BOTTLE, DROPPERSOLUTION28
0065-0817-02atropine sulfate1 in 1 CARTONSOLUTION18

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0065-0817ATROPINE SULFATE SOLUTION [ALCON LABORATORIES, INC.]6Current NDC, Legacy NDC, 4 package rows20250124_c8093125-ed1a-4eb6-9c81-52c5c7376481.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1190655atropine sulfate 1 % Ophthalmic SolutionPSNc8093125-ed1a-4eb6-9c81-52c5c73764818
1190655atropine sulfate 10 MG/ML Ophthalmic SolutionSCDc8093125-ed1a-4eb6-9c81-52c5c73764818
1190655atropine sulfate 1 % Ophthalmic SolutionSYc8093125-ed1a-4eb6-9c81-52c5c73764818

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0065-0817-01000650817011 BOTTLE, DROPPER in 1 CARTON (0065-0817-01) / 5 mL in 1 BOTTLE, DROPPER2022-11-010000-00-00NoNoCurrent
0065-0817-02000650817021 BOTTLE, DROPPER in 1 CARTON (0065-0817-02) / 2 mL in 1 BOTTLE, DROPPER2022-11-010000-00-00NoNoCurrent
0065-0817-03000650817031 BOTTLE, DROPPER in 1 CARTON (0065-0817-03) > 15 mL in 1 BOTTLE, DROPPER2022-05-010000-00-00NoNoCurrent