Wavelength Pharmaceuticals
NDC Database

Wavelength Pharmaceuticals

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 41
  • Latest Marketing Date 2025-01-12
  • Data Source FDA
  • First Marketing Date 2000-01-01
Company Overview

Company

Wavelength Pharmaceuticals

Country

Israel

Social Profiles

LinkedIn
Company Snapshot

Wavelength Pharmaceuticals

Ofer Park, Brosh building, 4th floor 94 Shlomo Shmeltzer Road, POB 3158, Petah, Tikva 4970602

Israel

www.wavelengthpharma.com/ PAPI@seqens.com View on Map
NDC Records ( 41 records )
2001
09 Feb
Bulk Ingredient NDC: 58175-0348

Nonproprietary Name

fenofibrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0348

Substance

FENOFIBRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2001-02-09

End Marketing Date

2027-04-30

Listing Record Certified Through

-

2001
09 Feb
Bulk Ingredient NDC: 58175-0350

Nonproprietary Name

midazolam base

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0350

Substance

MIDAZOLAM

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

2001-02-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2006
26 Apr
Bulk Ingredient NDC: 58175-0360

Nonproprietary Name

GRANISETRON HYDROCHLORIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0360

Substance

GRANISETRON HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2006-04-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2000
01 Jan
Bulk Ingredient NDC: 58175-0361

Nonproprietary Name

fluticasone propionate

Dosage Form

POWDER

Strength

1 g/g

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0361

Substance

FLUTICASONE PROPIONATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2000-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2001
01 Jan
Bulk Ingredient NDC: 58175-0364

Nonproprietary Name

tramadol hcl

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0364

Substance

TRAMADOL HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

2001-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2001
09 Feb
Bulk Ingredient NDC: 58175-0365

Nonproprietary Name

flumazenil

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0365

Substance

FLUMAZENIL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2001-02-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2001
09 Feb
Bulk Ingredient NDC: 58175-0370

Nonproprietary Name

cetirizine hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0370

Substance

CETIRIZINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2001-02-09

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2001
09 Feb
Bulk Ingredient NDC: 58175-0378

Nonproprietary Name

modafinil

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0378

Substance

MODAFINIL

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

2001-02-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2001
09 Feb
Bulk Ingredient NDC: 58175-0379

Nonproprietary Name

cilostazol

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0379

Substance

CILOSTAZOL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2001-02-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2005
06 Feb
Bulk Ingredient NDC: 58175-0391

Nonproprietary Name

halobetasol propionate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0391

Substance

HALOBETASOL PROPIONATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2005-02-06

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2004
27 Feb
Bulk Ingredient NDC: 58175-0395

Nonproprietary Name

rocuronium bromide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0395

Substance

ROCURONIUM BROMIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2004-02-27

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2004
16 Sep
Bulk Ingredient NDC: 58175-0397

Nonproprietary Name

imiquimod

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0397

Substance

IMIQUIMOD

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2004-09-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2001
09 Feb
Bulk Ingredient NDC: 58175-0407

Nonproprietary Name

pramipexole dihydrochloride monohydrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0407

Substance

PRAMIPEXOLE DIHYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2001-02-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2005
18 May
Bulk Ingredient NDC: 58175-0411

Nonproprietary Name

temozolomide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0411

Substance

TEMOZOLOMIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2005-05-18

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2006
04 Apr
Bulk Ingredient NDC: 58175-0537

Nonproprietary Name

granisetron base

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0537

Substance

GRANISETRON

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2006-04-04

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2010
30 Apr
Bulk Ingredient NDC: 58175-0541

Nonproprietary Name

cisatracurium besylate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0541

Substance

CISATRACURIUM BESYLATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-04-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2008
11 Feb
Bulk Ingredient NDC: 58175-0543

Nonproprietary Name

PALONOSETRON HYDROCHLORIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0543

Substance

PALONOSETRON HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2008-02-11

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2010
07 Jun
Bulk Ingredient NDC: 58175-0545

Nonproprietary Name

ROTIGOTINE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0545

Substance

ROTIGOTINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-06-07

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2006
21 Jun
Bulk Ingredient NDC: 58175-0549

Nonproprietary Name

donepezil base

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0549

Substance

DONEPEZIL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2006-06-21

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
04 Feb
Bulk Ingredient NDC: 58175-0551

Nonproprietary Name

MOMETASONE FUROATE MONOHYDRATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0551

Substance

MOMETASONE FUROATE MONOHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-02-04

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
25 Mar
Bulk Ingredient NDC: 58175-0553

Nonproprietary Name

fluticasone furoate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0553

Substance

FLUTICASONE FUROATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-03-25

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
05 Aug
Bulk Ingredient NDC: 58175-0557

Nonproprietary Name

Donepezil HCl

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0557

Substance

DONEPEZIL HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-08-05

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2010
15 Apr
Bulk Ingredient NDC: 58175-0559

Nonproprietary Name

OMEPRAZOLE MAGNESIUM

Dosage Form

POWDER

Strength

50 kg/50kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0559

Substance

OMEPRAZOLE MAGNESIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-04-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
12 Dec
Bulk Ingredient NDC: 58175-0565

Nonproprietary Name

Tiotropium Bromide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0565

Substance

TIOTROPIUM BROMIDE ANHYDROUS

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-12-12

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
01 Aug
Bulk Ingredient NDC: 58175-0600

Nonproprietary Name

fulvestrant

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0600

Substance

FULVESTRANT

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-08-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
30 Dec
Bulk Ingredient NDC: 58175-0602

Nonproprietary Name

ibrutinib

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0602

Substance

IBRUTINIB

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-12-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2015
15 May
Bulk Ingredient NDC: 58175-0604

Nonproprietary Name

permethrin

Dosage Form

LIQUID

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0604

Substance

PERMETHRIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2015-05-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2015
15 May
Bulk Ingredient NDC: 58175-0606

Nonproprietary Name

efinaconazole

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0606

Substance

EFINACONAZOLE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2015-05-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
15 Aug
Bulk Ingredient NDC: 58175-0614

Nonproprietary Name

tavaborole

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0614

Substance

TAVABOROLE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-08-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
30 Nov
Bulk Ingredient NDC: 58175-0616

Nonproprietary Name

fexofenadine hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0616

Substance

FEXOFENADINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-11-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2018
30 Aug
Bulk Ingredient NDC: 58175-0618

Nonproprietary Name

Sugammadex

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-0618

Substance

SUGAMMADEX

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2018-08-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
01 Apr
Bulk Ingredient NDC: 58175-0620

Nonproprietary Name

SITAGLIPTIN PHOSPHATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises Ltd

Marketing Category

BULK INGREDIENT

58175-0620

Substance

SITAGLIPTIN PHOSPHATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-04-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
01 Apr
Bulk Ingredient NDC: 58175-0622

Nonproprietary Name

Crisaborole

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises Ltd

Marketing Category

BULK INGREDIENT

58175-0622

Substance

CRISABOROLE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-04-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
01 Apr
Bulk Ingredient NDC: 58175-0624

Nonproprietary Name

Glycopyrronium Bromide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises Ltd

Marketing Category

BULK INGREDIENT

58175-0624

Substance

CHLOROGLYCOPYRRONIUM BROMIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-04-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
01 Apr
Bulk Ingredient NDC: 58175-0626

Nonproprietary Name

UMECLIDINIUM BROMIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises Ltd

Marketing Category

BULK INGREDIENT

58175-0626

Substance

UMECLIDINIUM BROMIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-04-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
01 Jun
Bulk Ingredient NDC: 58175-0628

Nonproprietary Name

Naltrexone Base

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises Ltd

Marketing Category

BULK INGREDIENT

58175-0628

Substance

NALTREXONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-06-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
31 Aug
Bulk Ingredient NDC: 58175-0648

Nonproprietary Name

REMIMAZOLAM BESYLATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises Ltd

Marketing Category

BULK INGREDIENT

58175-0648

Substance

REMIMAZOLAM BESYLATE

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

2022-08-31

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
30 Dec
Bulk Ingredient NDC: 58175-0650

Nonproprietary Name

CLASCOTERONE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises Ltd

Marketing Category

BULK INGREDIENT

58175-0650

Substance

CLASCOTERONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-12-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
15 Nov
Bulk Ingredient NDC: 58175-0654

Nonproprietary Name

GANAXOLONE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises Ltd

Marketing Category

BULK INGREDIENT

58175-0654

Substance

GANAXOLONE

Product Type

BULK INGREDIENT

DEA Schedule

CV

Start Marketing Date

2023-11-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
12 Jan
Bulk Ingredient NDC: 58175-0664

Nonproprietary Name

PODOFILOX

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

WAVELENGTH ENTERPRISES LTD

Marketing Category

BULK INGREDIENT

58175-0664

Substance

PODOFILOX

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-01-12

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2001
09 Feb
Bulk Ingredient NDC: 58175-1234

Nonproprietary Name

MOMETASONE FUROATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wavelength Enterprises LTD

Marketing Category

BULK INGREDIENT

58175-1234

Substance

MOMETASONE FUROATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2001-02-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
41 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

58175-0348

Nonproprietary Name

fenofibrate

Labeler

Wavelength Enterprises LTD

Dosage Form

POWDER

FDA NDC Data

National Drug Code information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

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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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