NDC 66096-122 Ohm Pituitarum Complex
Adrenal Gland,Adrenocorticotrophin,Cerebrum,Liver Gland,Pituitarum Posterium - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 66096 - Ohm Pharma Inc.
- 66096-122 - Ohm Pituitarum Complex
Product Packages
NDC Code 66096-122-05
Package Description: 59 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 66096-122?
What are Ohm Pituitarum Complex Active Ingredients?
- CORTICOTROPIN 10 [hp_X]/59mL
- EPINEPHRINE 10 [hp_X]/59mL - The active sympathomimetic hormone from the ADRENAL MEDULLA. It stimulates both the alpha- and beta- adrenergic systems, causes systemic VASOCONSTRICTION and gastrointestinal relaxation, stimulates the HEART, and dilates BRONCHI and cerebral vessels. It is used in ASTHMA and CARDIAC FAILURE and to delay absorption of local ANESTHETICS.
- SUS SCROFA ADRENAL GLAND 10 [hp_X]/59mL
- SUS SCROFA CEREBRUM 14 [hp_X]/59mL
- SUS SCROFA PITUITARY GLAND, POSTERIOR 10 [hp_X]/59mL
- SUS SCROFA PLACENTA 8 [hp_X]/59mL
- THYROID, UNSPECIFIED 8 [hp_X]/59mL
Which are Ohm Pituitarum Complex UNII Codes?
The UNII codes for the active ingredients in this product are:
- EPINEPHRINE (UNII: YKH834O4BH)
- EPINEPHRINE (UNII: YKH834O4BH) (Active Moiety)
- CORTICOTROPIN (UNII: K0U68Q2TXA)
- CORTICOTROPIN (UNII: K0U68Q2TXA) (Active Moiety)
- SUS SCROFA CEREBRUM (UNII: 4GB5DQR532)
- SUS SCROFA CEREBRUM (UNII: 4GB5DQR532) (Active Moiety)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (Active Moiety)
- SUS SCROFA PITUITARY GLAND, POSTERIOR (UNII: E8S87O660T)
- SUS SCROFA PITUITARY GLAND, POSTERIOR (UNII: E8S87O660T) (Active Moiety)
- SUS SCROFA PLACENTA (UNII: C8CV8867O8)
- SUS SCROFA PLACENTA (UNII: C8CV8867O8) (Active Moiety)
- THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P)
- THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P) (Active Moiety)
Which are Ohm Pituitarum Complex 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
Which are the Pharmacologic Classes for Ohm Pituitarum Complex?
- Adrenergic alpha-Agonists - [MoA] (Mechanism of Action)
- Adrenergic beta-Agonists - [MoA] (Mechanism of Action)
- Adrenocorticotropic Hormone - [CS]
- Adrenocorticotropic Hormone - [EPC] (Established Pharmacologic Class)
- Catecholamine - [EPC] (Established Pharmacologic Class)
- Catecholamines - [CS]
- alpha-Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
- beta-Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
* 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.
[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".