NDC 68151-3071 Propranolol Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68151 - Carilion Materials Management
- 68151-3071 - Propranolol Hydrochloride
Product Characteristics
WHITE (C48325)
Product Packages
NDC Code 68151-3071-1
Package Description: 1 CAPSULE, EXTENDED RELEASE in 1 PACKAGE
Product Details
What is NDC 68151-3071?
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:
- GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
- HYDROXYPROPYL CELLULOSE (1200000 MW) (UNII: RFW2ET671P)
- POVIDONE K30 (UNII: U725QWY32X)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ETHYLCELLULOSE, UNSPECIFIED (UNII: 7Z8S9VYZ4B)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- SUCROSE (UNII: C151H8M554)
- STARCH, CORN (UNII: O8232NY3SJ)
What is the NDC to RxNorm Crosswalk for Propranolol Hydrochloride?
- RxCUI: 856535 - propranolol HCl 60 MG 24HR Extended Release Oral Capsule
- RxCUI: 856535 - 24 HR propranolol hydrochloride 60 MG Extended Release Oral Capsule
- RxCUI: 856535 - propranolol hydrochloride 60 MG 24 HR Extended Release Oral Capsule
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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".