NDC 52533-056 Oxytocin
NDC Product Code 52533-056
Proprietary Name: Oxytocin What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NDC Code Structure
- 52533 - Cantrell Drug Company
- 52533-056 - Oxytocin
NDC 52533-056-18
Package Description: 250 mL in 1 BAG
NDC 52533-056-30
Package Description: 500 mL in 1 BAG
NDC Product Information
Oxytocin with NDC 52533-056 is product labeled by Cantrell Drug Company. The product's dosage form is and is administered via form.
Inactive Ingredient(s)
About the Inactive Ingredient(s)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.
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- WATER (UNII: 059QF0KO0R)
Product Labeler Information
What is the Labeler Name?Name of Company corresponding to the labeler code segment of the Product NDC.
Labeler Name: Cantrell Drug Company
Labeler Code: 52533
Start Marketing Date: 10-20-2011 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2017 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.
Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. 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".
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