NDC 71053-590 N/a
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71053 - Rafa Laboratories, Ltd.
- 71053-590 - N/a
Product Packages
NDC Code 71053-590-01
Package Description: .7 mL in 1 SYRINGE
Product Details
What is NDC 71053-590?
What are the uses for N/a?
Which are N/a UNII Codes?
The UNII codes for the active ingredients in this product are:
- ATROPINE (UNII: 7C0697DR9I)
- ATROPINE (UNII: 7C0697DR9I) (Active Moiety)
What is the NDC to RxNorm Crosswalk for N/a?
- RxCUI: 1190538 - atropine sulfate 0.5 MG in 0.7 ML Auto-Injector
- RxCUI: 1190538 - 0.7 ML atropine sulfate 0.714 MG/ML Auto-Injector
- RxCUI: 1190538 - atropine sulfate 0.5 MG (atropine 0.42 MG) per 0.7 ML Auto-Injector
- RxCUI: 1190540 - atropine sulfate 1 MG in 0.7 ML Auto-Injector
- RxCUI: 1190540 - 0.7 ML atropine sulfate 1.43 MG/ML Auto-Injector
* Please review the disclaimer below.
[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".