phenohytro

Generic: phenobarbital, hyoscyamine sulfate, atropine sulfate, and scopolamine hydrobromide

Labeler: atlantic biologicals corp.
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name phenohytro
Generic Name phenobarbital, hyoscyamine sulfate, atropine sulfate, and scopolamine hydrobromide
Labeler atlantic biologicals corp.
Dosage Form ELIXIR
Routes
ORAL
Active Ingredients

atropine sulfate .0194 mg/5mL, hyoscyamine sulfate .1037 mg/5mL, phenobarbital 16.2 mg/5mL, scopolamine hydrobromide .0065 mg/5mL

Manufacturer
ATLANTIC BIOLOGICALS CORP.

Identifiers & Regulatory

Product NDC 17856-0125
Product ID 17856-0125_3f64cdfa-e6e2-00c2-e063-6394a90abfea
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2018-08-30

Pharmacologic Class

Classes
anticholinergic [epc] cholinergic antagonists [moa] cholinergic muscarinic antagonist [epc] cholinergic muscarinic antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 178560125
Hyphenated Format 17856-0125

Supplemental Identifiers

RxCUI
1046787 2048017
UNII
03J5ZE7KA5 F2R8V82B84 YQE403BP4D 451IFR0GXB

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name phenohytro (source: ndc)
Generic Name phenobarbital, hyoscyamine sulfate, atropine sulfate, and scopolamine hydrobromide (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .0194 mg/5mL
  • .1037 mg/5mL
  • 16.2 mg/5mL
  • .0065 mg/5mL
source: ndc
Packaging
  • 72 CUP, UNIT-DOSE in 1 BOX (17856-0125-1) / 10 mL in 1 CUP, UNIT-DOSE (17856-0125-3)
  • 72 CUP, UNIT-DOSE in 1 BOX (17856-0125-2) / 5 mL in 1 CUP, UNIT-DOSE (17856-0125-4)
source: ndc

Packages (2)

Ingredients (4)

atropine sulfate (.0194 mg/5mL) hyoscyamine sulfate (.1037 mg/5mL) phenobarbital (16.2 mg/5mL) scopolamine hydrobromide (.0065 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3f64cdfa-e6e2-00c2-e063-6394a90abfea", "openfda": {"unii": ["03J5ZE7KA5", "F2R8V82B84", "YQE403BP4D", "451IFR0GXB"], "rxcui": ["1046787", "2048017"], "spl_set_id": ["a5aaf1db-1938-4073-9da4-c47f959d013e"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "72 CUP, UNIT-DOSE in 1 BOX (17856-0125-1)  / 10 mL in 1 CUP, UNIT-DOSE (17856-0125-3)", "package_ndc": "17856-0125-1", "marketing_start_date": "20240408"}, {"sample": false, "description": "72 CUP, UNIT-DOSE in 1 BOX (17856-0125-2)  / 5 mL in 1 CUP, UNIT-DOSE (17856-0125-4)", "package_ndc": "17856-0125-2", "marketing_start_date": "20240408"}], "brand_name": "Phenohytro", "product_id": "17856-0125_3f64cdfa-e6e2-00c2-e063-6394a90abfea", "dosage_form": "ELIXIR", "pharm_class": ["Anticholinergic [EPC]", "Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]", "Cholinergic Antagonists [MoA]", "Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "17856-0125", "dea_schedule": "CIV", "generic_name": "Phenobarbital, Hyoscyamine Sulfate, Atropine sulfate, and Scopolamine Hydrobromide", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenohytro", "active_ingredients": [{"name": "ATROPINE SULFATE", "strength": ".0194 mg/5mL"}, {"name": "HYOSCYAMINE SULFATE", "strength": ".1037 mg/5mL"}, {"name": "PHENOBARBITAL", "strength": "16.2 mg/5mL"}, {"name": "SCOPOLAMINE HYDROBROMIDE", "strength": ".0065 mg/5mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20180830", "listing_expiration_date": "20261231"}