NDC 50268-118 Atropine Sulfate
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What is NDC 50268-118?
What are the uses for Atropine Sulfate?
Which are Atropine Sulfate UNII Codes?
The UNII codes for the active ingredients in this product are:
- ATROPINE SULFATE (UNII: 03J5ZE7KA5)
- ATROPINE (UNII: 7C0697DR9I) (Active Moiety)
Which are Atropine Sulfate Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- LANOLIN OIL (UNII: OVV5IIJ58F)
- MINERAL OIL (UNII: T5L8T28FGP)
- WATER (UNII: 059QF0KO0R)
- PETROLATUM (UNII: 4T6H12BN9U)
What is the NDC to RxNorm Crosswalk for Atropine Sulfate?
- RxCUI: 1190570 - atropine sulfate 1 % Ophthalmic Ointment
- RxCUI: 1190570 - atropine sulfate 0.01 MG/MG Ophthalmic Ointment
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Patient Education
Atropine Ophthalmic
Ophthalmic atropine is used before eye examinations to dilate (open) the pupil, the black part of the eye through which you see. It is also used to relieve pain caused by swelling and inflammation of the eye.
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".