NDC 63304-822 Clarithromycin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63304 - Ranbaxy Pharmaceuticals Inc.
- 63304-822 - Clarithromycin
Product Characteristics
WHITE (C48325 - WHITE TO OFF-WHITE SUSPENSION)
18 MM
RX;726
TUTTI FRUTTI (C73420)
Product Packages
NDC Code 63304-822-03
Package Description: 50 mL in 1 BOTTLE
NDC Code 63304-822-04
Package Description: 100 mL in 1 BOTTLE
Product Details
What is NDC 63304-822?
What are the uses for Clarithromycin?
Which are Clarithromycin UNII Codes?
The UNII codes for the active ingredients in this product are:
- CLARITHROMYCIN (UNII: H1250JIK0A)
- CLARITHROMYCIN (UNII: H1250JIK0A) (Active Moiety)
Which are Clarithromycin 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:
- COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- POVIDONE (UNII: FZ989GH94E)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SHELLAC (UNII: 46N107B71O)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- ALGINIC ACID (UNII: 8C3Z4148WZ)
- ASPARTAME (UNII: Z0H242BBR1)
- CASTOR OIL (UNII: D5340Y2I9G)
- HYPROMELLOSE PHTHALATE (24% PHTHALATE, 55 CST) (UNII: 87Y6436BKR)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SUCROSE (UNII: C151H8M554)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
What is the NDC to RxNorm Crosswalk for Clarithromycin?
- RxCUI: 197516 - clarithromycin 250 MG Oral Tablet
- RxCUI: 197517 - clarithromycin 500 MG Oral Tablet
- RxCUI: 240741 - clarithromycin 125 MG in 5 mL Oral Suspension
- RxCUI: 240741 - clarithromycin 25 MG/ML Oral Suspension
- RxCUI: 240741 - clarithromycin 125 MG per 5 ML Oral Suspension
* 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".