NDC 17856-0125

Phenohytro

Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, And Scopolamine Hydrobromide

Phenohytro is a Oral Elixir in the Human Prescription Drug category. It is labeled and distributed by Atlantic Biologicals Corp.. The primary component is Phenobarbital; Hyoscyamine Sulfate; Atropine Sulfate; Scopolamine Hydrobromide.

• Product ID: 17856-0125_1866665a-4045-4842-a9f3-d32e3485a27f
• NDC: 17856-0125
• Product Type: Human Prescription Drug
• Proprietary Name: Phenohytro
• Generic Name: Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, And Scopolamine Hydrobromide
• Dosage Form: Elixir
• Route of Administration: ORAL
• Marketing Start Date: 2018-08-30
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: ATLANTIC BIOLOGICALS CORP.
• Substance Name: PHENOBARBITAL; HYOSCYAMINE SULFATE; ATROPINE SULFATE; SCOPOLAMINE HYDROBROMIDE
• Active Ingredient Strength: 16 mg/5mL; mg/5mL; mg/5mL; mg/5mL
• Pharm Classes: Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA],Anticholinergic [EPC],Cholinergic Antagonists [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 17856-0125-1

72 CUP, UNIT-DOSE in 1 BOX (17856-0125-1) > 10 mL in 1 CUP, UNIT-DOSE

• Marketing Start Date: 2020-05-20
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 17856-0125-1 [17856012501]

Phenohytro ELIXIR

• Marketing Category: UNAPPROVED DRUG OTHER
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2020-05-20
• Inactivation Date: 2020-01-31
• Reactivation Date: 2020-05-20

NDC 17856-0125-2 [17856012502]

Phenohytro ELIXIR

• Marketing Category: UNAPPROVED DRUG OTHER
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2020-05-20
• Inactivation Date: 2020-01-31
• Reactivation Date: 2020-05-20

Drug Details

Active Ingredients

Ingredient	Strength
PHENOBARBITAL	16.2 mg/5mL

OpenFDA Data

• SPL SET ID: a5aaf1db-1938-4073-9da4-c47f959d013e
• Manufacturer:
  • ATLANTIC BIOLOGICALS CORP.
• UNII:
  • YQE403BP4D
  • 451IFR0GXB
  • 03J5ZE7KA5
  • F2R8V82B84
• RxNorm Concept Unique ID - RxCUI:
  • 2048017
  • 1046787

Pharmacological Class

• Anticholinergic [EPC]
• Cholinergic Antagonists [MoA]
• Cholinergic Muscarinic Antagonist [EPC]
• Cholinergic Muscarinic Antagonists [MoA]
• Anticholinergic [EPC]
• Cholinergic Antagonists [MoA]

NDC Crossover Matching brand name "Phenohytro" or generic name "Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, And Scopolamine Hydrobromide"

NDC	Brand Name	Generic Name
17856-0123	Phenohytro	Phenobarbital, Hyoscyamine Sulfate, Atropine sulfate, and Scopolamine Hydrobromide
17856-0125	Phenohytro	Phenobarbital, Hyoscyamine Sulfate, Atropine sulfate, and Scopolamine Hydrobromide
75826-118	Phenohytro	PHENOBARBITAL, HYOSCYAMINE SULFATE, ATROPINE SULFATE, SCOPOLAMINE HYDROBROMIDE
75826-127	Phenohytro	Phenobarbital, Hyoscyamine Sulfate, Atropine sulfate, and Scopolamine Hydrobromide
75826-128	Phenohytro	Phenobarbital, Hyoscyamine Sulfate, Atropine sulfate, and Scopolamine Hydrobromide