NDC 50332-0103 Cetafen
NDC Product Code 50332-0103
Proprietary Name: Cetafen 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.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
NDC Code Structure
- 50332 - Hart Health
- 50332-0103 - Cetafen
NDC 50332-0103-1
Package Description: 500 PACKET in 1 BOX, UNIT-DOSE > 2 TABLET in 1 PACKET
NDC 50332-0103-4
Package Description: 50 PACKET in 1 BOX, UNIT-DOSE > 2 TABLET in 1 PACKET
NDC 50332-0103-7
Package Description: 125 PACKET in 1 BOX, UNIT-DOSE > 2 TABLET in 1 PACKET
NDC 50332-0103-8
Package Description: 250 PACKET in 1 BOX, UNIT-DOSE > 2 TABLET in 1 PACKET
NDC Product Information
Cetafen with NDC 50332-0103 is a product labeled by Hart Health. The generic name of Cetafen is . The product's dosage form is and is administered via form.
Dosage Form: -
Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
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.
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POVIDONE (UNII: FZ989GH94E)
- STEARIC ACID (UNII: 4ELV7Z65AP)
Product Labeler Information
What is the Labeler Name?Name of Company corresponding to the labeler code segment of the Product NDC.
Labeler Name: Hart Health
Labeler Code: 50332
Start Marketing Date: 06-04-1986 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: 12-31-2020 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: E 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. Values = ‘Y’ or ‘N’.
* Please review the disclaimer below.
Information for Patients
Acetaminophen
Acetaminophen is pronounced as (a set a mee' noe fen)
Why is acetaminophen medication prescribed?
Acetaminophen is used to relieve mild to moderate pain from headaches, muscle aches, menstrual periods, colds and sore throats, toothaches, backaches, and reactions to va...
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