Sterling Spa
NDC Database

Sterling Spa

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 2026-04-22
  • Data Source FDA
  • First Marketing Date 2010-10-19
Company Overview

Company

Sterling Spa

Country

Italy

Social Profiles

Company Snapshot

Sterling Spa

Solomeo di Corciano - Perugia

Italy

www.sterling.it/en/ info@sterling.it View on Map
NDC Records ( 41 records )
2010
19 Oct
Bulk Ingredient NDC: 64918-0331

Nonproprietary Name

MOMETASONE FUROATE MONOHYDRATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-0331

Substance

MOMETASONE FUROATE MONOHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-10-19

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
01 Jan
Bulk Ingredient NDC: 64918-0422

Nonproprietary Name

FINASTERIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-0422

Substance

FINASTERIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2015
01 Jan
Bulk Ingredient NDC: 64918-0428

Nonproprietary Name

DESOXYCORTICOSTERONE PIVALATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-0428

Substance

DESOXYCORTICOSTERONE PIVALATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2015-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
13 Nov
Bulk Ingredient NDC: 64918-0430

Nonproprietary Name

DESOXYCORTICOSTERONE PIVALATE

Dosage Form

INHALANT

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-0430

Substance

DESOXYCORTICOSTERONE PIVALATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-11-13

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
24 Jul
Bulk Ingredient NDC: 64918-0621

Nonproprietary Name

EXEMESTANE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-0621

Substance

EXEMESTANE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-07-24

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
01 Jan
Bulk Ingredient NDC: 64918-0706

Nonproprietary Name

FINASTERIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-0706

Substance

FINASTERIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
01 Jan
Bulk Ingredient NDC: 64918-0725

Nonproprietary Name

TRILOSTANE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-0725

Substance

TRILOSTANE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
09 Nov
Bulk Ingredient NDC: 64918-1002

Nonproprietary Name

NOMEGESTROL ACETATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1002

Substance

NOMEGESTROL ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-11-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
01 Jan
Bulk Ingredient NDC: 64918-1004

Nonproprietary Name

NOMEGESTROL ACETATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1004

Substance

NOMEGESTROL ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
24 Jul
Bulk Ingredient NDC: 64918-1031

Nonproprietary Name

DUTASTERIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1031

Substance

DUTASTERIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-07-24

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
13 Nov
Bulk Ingredient NDC: 64918-1117

Nonproprietary Name

FLUTICASONE FUROATE

Dosage Form

INHALANT

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1117

Substance

FLUTICASONE FUROATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-11-13

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
10 Mar
Bulk Ingredient NDC: 64918-1118

Nonproprietary Name

FLUTICASONE PROPIONATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1118

Substance

FLUTICASONE PROPIONATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-03-10

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2010
11 Nov
Bulk Ingredient NDC: 64918-1400

Nonproprietary Name

NORGESTIMATE MICRONIZED

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1400

Substance

NORGESTIMATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-11-11

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2010
11 Nov
Bulk Ingredient NDC: 64918-1401

Nonproprietary Name

DROSPIRENONE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1401

Substance

DROSPIRENONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-11-11

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
30 Nov
Bulk Ingredient NDC: 64918-1402

Nonproprietary Name

FULVESTRANT

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1402

Substance

FULVESTRANT

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-11-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
30 Nov
Bulk Ingredient NDC: 64918-1403

Nonproprietary Name

ABIRATERONE ACETATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1403

Substance

ABIRATERONE ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-11-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
16 Apr
Bulk Ingredient NDC: 64918-1404

Nonproprietary Name

NORETHINDRONE ACETATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1404

Substance

NORETHINDRONE ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-04-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
11 Jul
Bulk Ingredient NDC: 64918-1405

Nonproprietary Name

ABIRATERONE ACETATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1405

Substance

ABIRATERONE ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-07-11

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
13 Nov
Bulk Ingredient NDC: 64918-1900

Nonproprietary Name

CICLESONIDE

Dosage Form

INHALANT

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1900

Substance

CICLESONIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-11-13

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
08 Mar
Bulk Ingredient NDC: 64918-1902

Nonproprietary Name

RUXOLITINIB

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1902

Substance

RUXOLITINIB

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-03-08

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
13 Nov
Bulk Ingredient NDC: 64918-1903

Nonproprietary Name

DROSPIRENONE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1903

Substance

DROSPIRENONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-11-13

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
13 Nov
Bulk Ingredient NDC: 64918-1904

Nonproprietary Name

DUTASTERIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1904

Substance

DUTASTERIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-11-13

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
13 Nov
Bulk Ingredient NDC: 64918-1905

Nonproprietary Name

DYDROGESTERONE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1905

Substance

DYDROGESTERONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-11-13

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
13 Nov
Bulk Ingredient NDC: 64918-1906

Nonproprietary Name

ETONOGESTREL

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1906

Substance

ETONOGESTREL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-11-13

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
14 Apr
Bulk Ingredient NDC: 64918-1907

Nonproprietary Name

LEVONORGESTREL ACETATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1907

Substance

LEVONORGESTREL ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-04-14

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
13 Nov
Bulk Ingredient NDC: 64918-1910

Nonproprietary Name

FLUTICASONE FUROATE

Dosage Form

INHALANT

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1910

Substance

FLUTICASONE FUROATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-11-13

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
13 Nov
Bulk Ingredient NDC: 64918-1912

Nonproprietary Name

MOMETASONE FUROATE MONOHYDRATE

Dosage Form

INHALANT

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1912

Substance

MOMETASONE FUROATE MONOHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-11-13

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
04 Jan
Bulk Ingredient NDC: 64918-1915

Nonproprietary Name

FLUTICASONE FUROATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1915

Substance

FLUTICASONE FUROATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-01-04

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
04 Jan
Bulk Ingredient NDC: 64918-1916

Nonproprietary Name

FLUTICASONE FUROATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1916

Substance

FLUTICASONE FUROATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-01-04

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
04 Jan
Bulk Ingredient NDC: 64918-1917

Nonproprietary Name

METHYLPREDNISOLONE SULEPTANATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1917

Substance

METHYLPREDNISOLONE SULEPTANATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-01-04

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
04 Jan
Bulk Ingredient NDC: 64918-1918

Nonproprietary Name

UMECLIDINIUM BROMIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1918

Substance

UMECLIDINIUM BROMIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-01-04

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
04 Jan
Bulk Ingredient NDC: 64918-1919

Nonproprietary Name

VILANTEROL TRIFENATATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1919

Substance

VILANTEROL TRIFENATATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-01-04

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
04 Jun
Bulk Ingredient NDC: 64918-1920

Nonproprietary Name

UMECLIDINIUM BROMIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1920

Substance

UMECLIDINIUM BROMIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-06-04

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
04 Jun
Bulk Ingredient NDC: 64918-1921

Nonproprietary Name

VILANTEROL TRIFENATATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1921

Substance

VILANTEROL TRIFENATATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-06-04

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
12 May
Bulk Ingredient NDC: 64918-1924

Nonproprietary Name

CABOZANTINIB

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1924

Substance

CABOZANTINIB

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-05-12

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
28 Aug
Bulk Ingredient NDC: 64918-1939

Nonproprietary Name

FLUTICASONE FUROATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1939

Substance

FLUTICASONE FUROATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-08-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
18 Dec
Bulk Ingredient NDC: 64918-1940

Nonproprietary Name

NORGESTREL

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1940

Substance

NORGESTREL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-12-18

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
15 Jan
Bulk Ingredient NDC: 64918-1941

Nonproprietary Name

MEDROXYPROGESTERONE ACETATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1941

Substance

MEDROXYPROGESTERONE ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-01-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
24 Jan
Bulk Ingredient NDC: 64918-1942

Nonproprietary Name

NILOTINIB TRIFLUOROACETATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-1942

Substance

NILOTINIB TRIFLUOROACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-01-24

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2026
27 Feb
Bulk Ingredient NDC: 64918-5929

Nonproprietary Name

ENSIFENTRINE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-5929

Substance

ENSIFENTRINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2026-02-27

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2026
22 Apr
Bulk Ingredient NDC: 64918-5930

Nonproprietary Name

ORFORGLIPRON HEMICALCIUM HYDRATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

STERLING SPA

Marketing Category

BULK INGREDIENT

64918-5930

Substance

ORFORGLIPRON HEMICALCIUM MONOHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2026-04-22

End Marketing Date

-

Listing Record Certified Through

2027-12-31

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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

64918-0331

Nonproprietary Name

MOMETASONE FUROATE MONOHYDRATE

Labeler

STERLING SPA

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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