Phenohytro 16.2 mg / 0.1037 mg / 0.0194 mg / 0.0065 mg in 5 mL Oral Solution
RxNorm 2048017 NDC Crossover

NDC Directory Crossover & Product Mapping

The following National Drug Codes (NDCs) are directly associated with the clinical concept for Phenohytro 16.2 mg / 0.1037 mg / 0.0194 mg / 0.0065 mg in 5 mL Oral Solution (RxCUI 2048017). This crossover tool provides a verified mapping between standardized RxNorm clinical drug definitions and the specific manufactured products listed in the FDA NDC directory.

Healthcare professionals, pharmacists, and data analysts use this list to identify various brand names, labelers, and commercial packaging variations linked to this semantic clinical drug concept. Each entry below represents a commercial product that fulfills the requirements of this specific clinical identifier.

Manufacturer Quick Index

→ ATLANTIC BIOLOGICALS CORP. 2
→ Winder Laboratories LLC 2

ATLANTIC BIOLOGICALS CORP.

NDC Product

Phenohytro
NDC 17856-0123

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED DRUG OTHER
Excluded / Inactive
NDC Product
Human Prescription Drug

Phenohytro
NDC 17856-0125

Generic Name
Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, And Scopolamine Hydrobromide
Dosage Form
Elixir
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Winder Laboratories LLC

NDC Product
Human Prescription Drug

Phenohytro
NDC 75826-127

Generic Name
Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, And Scopolamine Hydrobromide
Dosage Form
Elixir
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Phenohytro
NDC 75826-128

Generic Name
Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, And Scopolamine Hydrobromide
Dosage Form
Elixir
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing