NDC 50090-1815 Bicillin Cr
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-1815 - Bicillin Cr
Product Packages
NDC Code 50090-1815-0
Package Description: 10 SYRINGE in 1 PACKAGE / 2 mL in 1 SYRINGE
Product Details
What is NDC 50090-1815?
What are the uses for Bicillin Cr?
Which are Bicillin Cr UNII Codes?
The UNII codes for the active ingredients in this product are:
- PENICILLIN G BENZATHINE (UNII: RIT82F58GK)
- PENICILLIN G (UNII: Q42T66VG0C) (Active Moiety)
- PENICILLIN G PROCAINE (UNII: 17R794ESYN)
Which are Bicillin Cr 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:
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)
- POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Bicillin Cr?
- RxCUI: 731538 - penicillin G benzathine / penicillin G procaine 1,200,000 UNT (600,000 UNT/ 600,000 UNT) in 2 ML Prefilled Syringe
- RxCUI: 731538 - 2 ML penicillin G benzathine 300000 UNT/ML / penicillin G procaine 300000 UNT/ML Prefilled Syringe
- RxCUI: 731538 - penicillin G benzathine 600,000 UNT / penicillin G procaine 600000 UNT per 2 ML Prefilled Syringe
- RxCUI: 731541 - BICILLIN C-R 1,200,000 UNT in 2 ML Prefilled Syringe
- RxCUI: 731541 - 2 ML penicillin G benzathine 300000 UNT/ML / penicillin G procaine 300000 UNT/ML Prefilled Syringe [Bicillin]
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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".