NDC 68875-0204 Natpara (parathyroid Hormone)
Parathyroid Hormone Injection, Powder, Lyophilized, For Solution Subcutaneous - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68875 - Takeda Pharmaceuticals America, Inc.
- 68875-0204 - Natpara (parathyroid Hormone)
Product Packages
NDC Code 68875-0204-2
Package Description: 2 CARTRIDGE in 1 CARTON / 1.13 mL in 1 CARTRIDGE (68875-0204-1)
Product Details
What is NDC 68875-0204?
What are the uses for Natpara (parathyroid Hormone)?
What are Natpara (parathyroid Hormone) Active Ingredients?
- PARATHYROID HORMONE 75 ug/.08mL - A polypeptide hormone (84 amino acid residues) secreted by the PARATHYROID GLANDS which performs the essential role of maintaining intracellular CALCIUM levels in the body. Parathyroid hormone increases intracellular calcium by promoting the release of CALCIUM from BONE, increases the intestinal absorption of calcium, increases the renal tubular reabsorption of calcium, and increases the renal excretion of phosphates.
Which are Natpara (parathyroid Hormone) UNII Codes?
The UNII codes for the active ingredients in this product are:
- PARATHYROID HORMONE (UNII: N19A0T0E5J)
- PARATHYROID HORMONE (UNII: N19A0T0E5J) (Active Moiety)
Which are Natpara (parathyroid Hormone) 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:
- MANNITOL (UNII: 3OWL53L36A)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- WATER (UNII: 059QF0KO0R)
- METACRESOL (UNII: GGO4Y809LO)
What is the NDC to RxNorm Crosswalk for Natpara (parathyroid Hormone)?
- RxCUI: 1602023 - parathyroid hormone 25 MCG/Dose in 14 Dose Cartridge
- RxCUI: 1602023 - 14 ACTUAT parathyroid hormone 0.025 MG/ACTUAT Cartridge
- RxCUI: 1602023 - parathyroid hormone 0.025 MG/ACTUAT Cartridge, 14 ACTUAT
- RxCUI: 1602023 - parathyroid hormone 25 MCG/Dose Cartridge, 14 Doses
- RxCUI: 1602028 - Natpara 25 MCG/Dose in 14 Dose Cartridge
Which are the Pharmacologic Classes for Natpara (parathyroid Hormone)?
* Please review the disclaimer below.
Patient Education
Parathyroid Hormone Injection
Parathyroid hormone injection is used along with calcium and vitamin D to treat low levels of calcium in the blood in people with certain types of hypoparathyroidism (condition in which the body does not produce enough parathyroid hormone [PTH; a natural substance needed to control the amount of calcium in the blood].) Parathyroid hormone injection should not be used to treat low levels of calcium in the blood in people whose condition can be controlled by calcium and vitamin D alone. Parathyroid hormone injection is in a class of medications called hormones. It works by causing the body to absorb more calcium into the blood.
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* Please review the disclaimer below.
[1] 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.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] 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.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".