phenobarbital, hyoscyamine sulfate, atropine sulfate and scopolamine hydrobromide

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

Labeler: ingenus pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name phenobarbital, hyoscyamine sulfate, atropine sulfate and scopolamine hydrobromide
Generic Name phenobarbital, hyoscyamine sulfate, atropine sulfate and scopolamine hydrobromide
Labeler ingenus pharmaceuticals, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

atropine sulfate .0194 mg/1, hyoscyamine sulfate .1037 mg/1, phenobarbital 16.2 mg/1, scopolamine hydrobromide .0065 mg/1

Manufacturer
Ingenus Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 50742-667
Product ID 50742-667_3796f3d7-7e45-4a49-aaa2-7363c197b2f2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2021-08-01

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 50742667
Hyphenated Format 50742-667

Supplemental Identifiers

RxCUI
1046815
UPC
0350742667017
UNII
03J5ZE7KA5 F2R8V82B84 YQE403BP4D 451IFR0GXB

Packaging Origin

Original Packager
true

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

Resolved Composition

Strengths
  • .0194 mg/1
  • .1037 mg/1
  • 16.2 mg/1
  • .0065 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (50742-667-01)
source: ndc

Packages (1)

50742-667-01 100 TABLET in 1 BOTTLE, PLASTIC (50742-667-01)

Ingredients (4)

atropine sulfate (.0194 mg/1) hyoscyamine sulfate (.1037 mg/1) phenobarbital (16.2 mg/1) scopolamine hydrobromide (.0065 mg/1)

Linked Drug Pages (1)

Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate and Scopolamine Hydrobromide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3796f3d7-7e45-4a49-aaa2-7363c197b2f2", "openfda": {"upc": ["0350742667017"], "unii": ["03J5ZE7KA5", "F2R8V82B84", "YQE403BP4D", "451IFR0GXB"], "rxcui": ["1046815"], "spl_set_id": ["0dd71f55-e009-48dd-809d-5f651f7521de"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (50742-667-01)", "package_ndc": "50742-667-01", "marketing_start_date": "20210801"}], "brand_name": "Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate and Scopolamine Hydrobromide", "product_id": "50742-667_3796f3d7-7e45-4a49-aaa2-7363c197b2f2", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]", "Cholinergic Antagonists [MoA]", "Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "50742-667", "dea_schedule": "CIV", "generic_name": "Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate and Scopolamine Hydrobromide", "labeler_name": "Ingenus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate and Scopolamine Hydrobromide", "active_ingredients": [{"name": "ATROPINE SULFATE", "strength": ".0194 mg/1"}, {"name": "HYOSCYAMINE SULFATE", "strength": ".1037 mg/1"}, {"name": "PHENOBARBITAL", "strength": "16.2 mg/1"}, {"name": "SCOPOLAMINE HYDROBROMIDE", "strength": ".0065 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20210801", "listing_expiration_date": "20261231"}