HTL Biotechnology
NDC Database

HTL Biotechnology

NDC Database

National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.

Bulk Ingredient
  • Total Records 3
  • Latest Marketing Date 2025-02-15
  • Data Source FDA
  • First Marketing Date 2014-12-16
Company Overview

Company

HTL Biotechnology

Country

France

Website

Visit Website

Email

contact@htlbiotech.com

Social Profiles

LinkedIn
Company Snapshot

HTL Biotechnology

7 Rue Alfred Kastler - ZI de l’Aumaillerie 35133 Javene

France

htlbiotech.com/ contact@htlbiotech.com View on Map
NDC Records ( 3 records )
2014
16 Dec
Bulk Ingredient NDC: 51035-002

Nonproprietary Name

HYALURONATE SODIUM

Dosage Form

POWDER

Strength

1 g/g

Labeler

HTL

Marketing Category

BULK INGREDIENT

51035-002

Substance

HYALURONATE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-12-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
15 Feb
Bulk Ingredient NDC: 51035-003

Nonproprietary Name

SODIUM HYALURONATE

Dosage Form

SOLUTION

Strength

1 g/g

Labeler

HTL

Marketing Category

BULK INGREDIENT

51035-003

Substance

SODIUM HYALURONATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-02-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
16 Dec
Bulk Ingredient NDC: 51035-001

Nonproprietary Name

HYALURONATE SODIUM

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

HTL SAS

Marketing Category

BULK INGREDIENT

51035-001

Substance

HYALURONATE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-12-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
3 total
  • Bulk Ingredient
Official Source

NDC data is based on publicly available National Drug Code information from the U.S. Food and Drug Administration (FDA).

Visit FDA NDC Directory
NDC Record Details Preview

Explore important National Drug Code information available in the records above.

NDC

51035-002

Nonproprietary Name

HYALURONATE SODIUM

Labeler

HTL

Dosage Form

POWDER

FDA NDC Data

National Drug Code information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

Organized NDC records

NDC data is based on publicly available U.S. Food and Drug Administration (FDA) National Drug Code information.

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