Tamiflu 6 mg in 1 mL Oral Suspension
RxNorm 1115700 NDC Crossover

NDC Directory Crossover & Product Mapping

The following National Drug Codes (NDCs) are directly associated with the clinical concept for Tamiflu 6 mg in 1 mL Oral Suspension (RxCUI 1115700). 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

→ A-S Medication Solutions 1
→ Genentech, Inc. 4
→ Physicians Total Care, Inc. 3
→ Rebel Distributors Corp 1

A-S Medication Solutions

NDC Product

Tamiflu
NDC 50090-1244

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
NDA
Excluded / Inactive

Genentech, Inc.

NDC Product
Human Prescription Drug

Tamiflu
NDC 0004-0800

Generic Name
Oseltamivir Phosphate
Dosage Form
Capsule
Route
Oral
Marketing
NDA
Active Listing
NDC Product

Tamiflu
NDC 0004-0801

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Tamiflu
NDC 0004-0802

Generic Name
Oseltamivir Phosphate
Dosage Form
Capsule
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Tamiflu
NDC 0004-0822

Generic Name
Oseltamivir Phosphate
Dosage Form
Powder, For Suspension
Route
Oral
Marketing
NDA
Active Listing

Physicians Total Care, Inc.

NDC Product

Tamiflu
NDC 54868-4476

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
NDA
Excluded / Inactive
NDC Product

Tamiflu
NDC 54868-6083

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
NDA
Excluded / Inactive
NDC Product

Tamiflu
NDC 54868-6315

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
NDA
Excluded / Inactive

Rebel Distributors Corp

NDC Product

Tamiflu
NDC 42254-092

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
NDA
Excluded / Inactive