NDC 36987-1234 Oyster
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 36987 - Nelco Laboratories, Inc.
- 36987-1234 - Oyster
Product Packages
NDC Code 36987-1234-1
Package Description: 5 mL in 1 VIAL, MULTI-DOSE
NDC Code 36987-1234-2
Package Description: 10 mL in 1 VIAL, MULTI-DOSE
NDC Code 36987-1234-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE
NDC Code 36987-1234-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE
Product Details
What is NDC 36987-1234?
What are the uses for Oyster?
Which are Oyster UNII Codes?
The UNII codes for the active ingredients in this product are:
- COMMON CARP (UNII: ZB2SV6JJY5)
- COMMON CARP (UNII: ZB2SV6JJY5) (Active Moiety)
- CLAM (UNII: 226LY0AFR9)
- CLAM (UNII: 226LY0AFR9) (Active Moiety)
- CODFISH (UNII: 8D6Q5LNG3D)
- CODFISH (UNII: 8D6Q5LNG3D) (Active Moiety)
- CRAB (UNII: S1VF61QLO9)
- CRAB (UNII: S1VF61QLO9) (Active Moiety)
- FLOUNDER (UNII: T197LO581X)
- FLOUNDER (UNII: T197LO581X) (Active Moiety)
- HADDOCK (UNII: 0WLY635722)
- HADDOCK (UNII: 0WLY635722) (Active Moiety)
- PACIFIC HALIBUT (UNII: BKZ683617P)
- PACIFIC HALIBUT (UNII: BKZ683617P) (Active Moiety)
- HERRING (UNII: 34EX28T4C1)
- HERRING (UNII: 34EX28T4C1) (Active Moiety)
- LOBSTER (UNII: ZQ6LG2C39M)
- LOBSTER (UNII: ZQ6LG2C39M) (Active Moiety)
- MACKEREL (UNII: CYO6K3VM7F)
- MACKEREL (UNII: CYO6K3VM7F) (Active Moiety)
- OYSTER (UNII: S614XWR17V)
- OYSTER (UNII: S614XWR17V) (Active Moiety)
Which are Oyster 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:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- PHENOL (UNII: 339NCG44TV)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Oyster?
- RxCUI: 899412 - crab allergenic extract 50 MG/ML Injectable Solution
- RxCUI: 899412 - crab allergenic extract 0.05 GM/ML Injectable Solution
- RxCUI: 899412 - crab allergenic extract 1 GM per 20 ML Injectable Solution
- RxCUI: 899412 - crab extract 50 MG/ML Injectable Solution
- RxCUI: 899431 - haddock allergenic extract 50 MG/ML Injectable Solution
* 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".