Bachem AG
NDC Database

Bachem AG

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 50
  • Latest Marketing Date 2025-08-27
  • Data Source FDA
  • First Marketing Date 1991-07-11
Company Overview

Company

Bachem AG

Country

Switzerland

Social Profiles

LinkedIn X / Twitter
Company Snapshot

Bachem AG

Hauptstrasse 144, 4416 Bubendorf

Switzerland

www.bachem.com/ sales.ch@bachem.com View on Map
NDC Records ( 50 records )
2001
01 Nov
Bulk Ingredient NDC: 55463-0002

Nonproprietary Name

Leuprorelin

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem AG

Marketing Category

BULK INGREDIENT

55463-0002

Substance

LEUPROLIDE ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2001-11-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1999
13 Oct
Bulk Ingredient NDC: 55463-0004

Nonproprietary Name

Sincalide

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem AG

Marketing Category

BULK INGREDIENT

55463-0004

Substance

SINCALIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1999-10-13

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2003
25 Nov
Bulk Ingredient NDC: 55463-0005

Nonproprietary Name

Goserelin

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem AG

Marketing Category

BULK INGREDIENT

55463-0005

Substance

GOSERELIN ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2003-11-25

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2006
21 Jun
Bulk Ingredient NDC: 55463-0006

Nonproprietary Name

Triptorelin Pamoate

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem AG

Marketing Category

BULK INGREDIENT

55463-0006

Substance

TRIPTORELIN PAMOATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2006-06-21

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2002
07 Mar
Bulk Ingredient NDC: 55463-0007

Nonproprietary Name

Triptorelin Acetate

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem AG

Marketing Category

BULK INGREDIENT

55463-0007

Substance

TRIPTORELIN ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2002-03-07

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2001
07 Jun
Bulk Ingredient NDC: 55463-0008

Nonproprietary Name

Histrelin Acetate

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem AG

Marketing Category

BULK INGREDIENT

55463-0008

Substance

HISTRELIN ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2001-06-07

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2005
10 Mar
Bulk Ingredient NDC: 55463-0009

Nonproprietary Name

Glucagon

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem AG

Marketing Category

BULK INGREDIENT

55463-0009

Substance

GLUCAGON

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2005-03-10

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2006
17 Nov
Bulk Ingredient NDC: 55463-0015

Nonproprietary Name

Tetracosactide

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem AG

Marketing Category

BULK INGREDIENT

55463-0015

Substance

COSYNTROPIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2006-11-17

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2003
06 Mar
Bulk Ingredient NDC: 55463-0016

Nonproprietary Name

Gonadorelin

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem AG

Marketing Category

BULK INGREDIENT

55463-0016

Substance

GONADORELIN ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2003-03-06

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2004
03 Mar
Bulk Ingredient NDC: 55463-0024

Nonproprietary Name

Buserelin

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem AG

Marketing Category

BULK INGREDIENT

55463-0024

Substance

BUSERELIN ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2004-03-03

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
27 Mar
Bulk Ingredient NDC: 55463-0029

Nonproprietary Name

Bivalirudin

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem AG

Marketing Category

BULK INGREDIENT

55463-0029

Substance

BIVALIRUDIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-03-27

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
24 Aug
Bulk Ingredient NDC: 55463-0030

Nonproprietary Name

ETELCALCETIDE

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem AG

Marketing Category

BULK INGREDIENT

55463-0030

Substance

ETELCALCETIDE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-08-24

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2007
26 Feb
Bulk Ingredient NDC: 55463-0031

Nonproprietary Name

Aprotinin

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem AG

Marketing Category

BULK INGREDIENT

55463-0031

Substance

APROTININ

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2007-02-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1994
01 Jan
Bulk Ingredient NDC: 55463-0032

Nonproprietary Name

PENTETREOTIDE

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem AG

Marketing Category

BULK INGREDIENT

55463-0032

Substance

PENTETREOTIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1994-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2007
17 Sep
Bulk Ingredient NDC: 55463-0033

Nonproprietary Name

Icatibant Acetate

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem AG

Marketing Category

BULK INGREDIENT

55463-0033

Substance

ICATIBANT ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2007-09-17

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2004
17 Aug
Bulk Ingredient NDC: 55463-0034

Nonproprietary Name

Nitisinone

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem AG

Marketing Category

BULK INGREDIENT

55463-0034

Substance

NITISINONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2004-08-17

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
11 Oct
Bulk Ingredient NDC: 55463-0035

Nonproprietary Name

Octreotide Acetate

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem AG

Marketing Category

BULK INGREDIENT

55463-0035

Substance

OCTREOTIDE ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-10-11

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
09 Dec
Bulk Ingredient NDC: 55463-0036

Nonproprietary Name

Pegcetacoplan

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem AG

Marketing Category

BULK INGREDIENT

55463-0036

Substance

PEGCETACOPLAN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-12-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
01 Jul
Bulk Ingredient NDC: 55463-0037

Nonproprietary Name

DASIGLUCAGON HYDROCHLORIDE

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem AG

Marketing Category

BULK INGREDIENT

55463-0037

Substance

DASIGLUCAGON HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-07-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
23 Oct
Bulk Ingredient NDC: 55463-0038

Nonproprietary Name

Octreotide Hydrochloride

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem AG

Marketing Category

BULK INGREDIENT

55463-0038

Substance

OCTREOTIDE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-10-23

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
15 Nov
Bulk Ingredient NDC: 55463-0039

Nonproprietary Name

Palopegteriparatide

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem AG

Marketing Category

BULK INGREDIENT

55463-0039

Substance

PALOPEGTERIPARATIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-11-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
30 Apr
Bulk Ingredient NDC: 55463-0040

Nonproprietary Name

Semaglutide

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem AG

Marketing Category

BULK INGREDIENT

55463-0040

Substance

SEMAGLUTIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-04-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
25 Feb
Bulk Ingredient NDC: 52416-095

Nonproprietary Name

CASIMERSEN

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem Americas, Inc.

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

52416-095

Substance

CASIMERSEN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-02-25

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1996
23 May
Bulk Ingredient NDC: 52416-102

Nonproprietary Name

Corticorelin Ovine Triflutate

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem Americas, Inc.

Marketing Category

BULK INGREDIENT

52416-102

Substance

CORTICORELIN OVINE TRIFLUTATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1996-05-23

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2005
28 Apr
Bulk Ingredient NDC: 52416-105

Nonproprietary Name

Exenatide

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem Americas, Inc.

Marketing Category

BULK INGREDIENT

52416-105

Substance

EXENATIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2005-04-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2005
16 May
Bulk Ingredient NDC: 52416-106

Nonproprietary Name

Pramlintide

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem Americas, Inc.

Marketing Category

BULK INGREDIENT

52416-106

Substance

PRAMLINTIDE ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2005-05-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2010
10 Nov
Bulk Ingredient NDC: 52416-107

Nonproprietary Name

Hexenoyl-hGRF 1-44

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem Americas, Inc.

Marketing Category

BULK INGREDIENT

52416-107

Substance

TESAMORELIN ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-11-10

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2001
27 Sep
Bulk Ingredient NDC: 52416-108

Nonproprietary Name

Desmopressin

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem Americas, Inc.

Marketing Category

EXPORT ONLY

52416-108

Substance

DESMOPRESSIN ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2001-09-27

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2018
06 Apr
Bulk Ingredient NDC: 52416-109

Nonproprietary Name

Octreotide

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem Americas, Inc.

Marketing Category

BULK INGREDIENT

52416-109

Substance

OCTREOTIDE ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2018-04-06

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2003
19 Nov
Bulk Ingredient NDC: 52416-110

Nonproprietary Name

Deslorelin

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem Americas, Inc.

Marketing Category

BULK INGREDIENT

52416-110

Substance

DESLORELIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2003-11-19

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
08 Jun
Bulk Ingredient NDC: 52416-111

Nonproprietary Name

Calcitonin Salmon

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem Americas, Inc.

Marketing Category

BULK INGREDIENT

52416-111

Substance

CALCITONIN SALMON

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-06-08

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2015
30 Sep
Bulk Ingredient NDC: 52416-120

Nonproprietary Name

AVI-4658

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem Americas, Inc.

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

52416-120

Substance

ETEPLIRSEN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2015-09-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
26 Jun
Bulk Ingredient NDC: 52416-123

Nonproprietary Name

Octreotide Acetate

Dosage Form

POWDER

Strength

1 g/g

Labeler

BACHEM AMERICAS, INC.

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

52416-123

Substance

OCTREOTIDE ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-06-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
19 Nov
Bulk Ingredient NDC: 52416-124

Nonproprietary Name

Exenatide

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem Americas, Inc.

Marketing Category

BULK INGREDIENT

52416-124

Substance

EXENATIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-11-19

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
22 Dec
Bulk Ingredient NDC: 52416-126

Nonproprietary Name

Teriparatide Acetate (hPTH (1-34))

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem Americas, Inc.

Marketing Category

EXPORT ONLY

52416-126

Substance

TERIPARATIDE ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-12-22

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
16 May
Bulk Ingredient NDC: 52416-127

Nonproprietary Name

Vasopressin

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem Americas, Inc.

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

52416-127

Substance

VASOPRESSIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-05-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
12 Dec
Bulk Ingredient NDC: 52416-128

Nonproprietary Name

GOLODIRSEN

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem Americas, Inc.

Marketing Category

BULK INGREDIENT

52416-128

Substance

GOLODIRSEN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-12-12

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
25 Feb
Bulk Ingredient NDC: 52416-129

Nonproprietary Name

CASIMERSEN

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem Americas, Inc.

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

52416-129

Substance

CASIMERSEN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-02-25

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
18 Feb
Bulk Ingredient NDC: 52416-130

Nonproprietary Name

AVI-4658

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem Americas, Inc.

Marketing Category

BULK INGREDIENT

52416-130

Substance

ETEPLIRSEN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-02-18

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
01 Jan
Bulk Ingredient NDC: 52416-131

Nonproprietary Name

LUM015 Acetate

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem Americas, Inc.

Marketing Category

BULK INGREDIENT

52416-131

Substance

PEGULICIANINE ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
12 Nov
Bulk Ingredient NDC: 52416-282

Nonproprietary Name

Golodirsen

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem Americas, Inc.

Marketing Category

BULK INGREDIENT

52416-282

Substance

GOLODIRSEN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-11-12

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
20 May
Bulk Ingredient NDC: 52416-640

Nonproprietary Name

AVI-4658 50L

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem Americas, Inc.

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

52416-640

Substance

ETEPLIRSEN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-05-20

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
27 Aug
Bulk Ingredient NDC: 52416-735

Nonproprietary Name

Liraglutide

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem Americas, Inc.

Marketing Category

BULK INGREDIENT

52416-735

Substance

LIRAGLUTIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-08-27

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
21 Nov
Bulk Ingredient NDC: 52416-777

Nonproprietary Name

Ziconotide

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem Americas, Inc.

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

52416-777

Substance

ZICONOTIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-11-21

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
10 Jul
Bulk Ingredient NDC: 52416-798

Nonproprietary Name

AVI-4658 250L

Dosage Form

POWDER

Strength

1 g/g

Labeler

Bachem Americas, Inc.

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

52416-798

Substance

ETEPLIRSEN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-07-10

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1991
11 Jul
Bulk Ingredient NDC: 51504-0001

Nonproprietary Name

CARBIDOPA

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Bachem SA, succursale de Vionnaz

Marketing Category

BULK INGREDIENT

51504-0001

Substance

CARBIDOPA

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1991-07-11

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1994
22 Nov
Bulk Ingredient NDC: 51504-0003

Nonproprietary Name

PROPOFOL

Dosage Form

LIQUID

Strength

1 kg/kg

Labeler

Bachem SA, succursale de Vionnaz

Marketing Category

BULK INGREDIENT

51504-0003

Substance

PROPOFOL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1994-11-22

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1992
25 Nov
Bulk Ingredient NDC: 51504-0005

Nonproprietary Name

5-Aminolevulinic Acid

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Bachem SA, succursale de Vionnaz

Marketing Category

BULK INGREDIENT

51504-0005

Substance

AMINOLEVULINIC ACID

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1992-11-25

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2007
29 Jan
Bulk Ingredient NDC: 51504-0012

Nonproprietary Name

ETOMIDATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Bachem SA, succursale de Vionnaz

Marketing Category

BULK INGREDIENT

51504-0012

Substance

ETOMIDATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2007-01-29

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
31 Mar
Bulk Ingredient NDC: 51504-0023

Nonproprietary Name

VILOXAZINE HYDROCHLORIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Bachem SA, succursale de Vionnaz

Marketing Category

BULK INGREDIENT

51504-0023

Substance

VILOXAZINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-03-31

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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

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NDC

55463-0002

Nonproprietary Name

Leuprorelin

Labeler

Bachem AG

Dosage Form

POWDER

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

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