NDC 50090-1969 Propranolol Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-1969 - Propranolol Hydrochloride
Product Characteristics
BLUE (C48333)
7 MM
PLIVA;468
Product Packages
NDC Code 50090-1969-1
Package Description: 100 TABLET in 1 BOTTLE
Product Details
What is NDC 50090-1969?
What are the uses for Propranolol Hydrochloride?
Which are Propranolol Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- PROPRANOLOL HYDROCHLORIDE (UNII: F8A3652H1V)
- PROPRANOLOL (UNII: 9Y8NXQ24VQ) (Active Moiety)
Which are Propranolol Hydrochloride 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:
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Propranolol Hydrochloride?
- RxCUI: 856457 - propranolol HCl 20 MG Oral Tablet
- RxCUI: 856457 - propranolol hydrochloride 20 MG Oral Tablet
- RxCUI: 856519 - propranolol HCl 40 MG Oral Tablet
- RxCUI: 856519 - propranolol hydrochloride 40 MG Oral Tablet
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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".