PolyPeptide Group
NDC Database
PolyPeptide Group
NDC Database
National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.
- Total Records 18
- Latest Marketing Date 2025-02-28
- Data Source FDA
- First Marketing Date 2010-01-01
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PolyPeptide Group
Dammstrasse 19 6300 Zug Switzerland
Switzerland
www.polypeptide.com/ sandiego@polypeptide.com View on MapNDC Records ( 18 records )
Nonproprietary Name
ZILUCOPLAN
Dosage Form
POWDER
Strength
1 g/g
Labeler
PolyPeptide Laboratories France
Marketing Category
BULK INGREDIENT
Substance
ZILUCOPLAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-01-10
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
MACIMORELIN ACETATE
Dosage Form
POWDER
Strength
1 g/g
Labeler
PolyPeptide Laboratories France
Marketing Category
BULK INGREDIENT
Substance
MACIMORELIN ACETATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-01-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
DIFELIKEFALIN
Dosage Form
POWDER
Strength
1 g/g
Labeler
PolyPeptide Laboratories France
Marketing Category
BULK INGREDIENT
Substance
DIFELIKEFALIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-01-08
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
linaclotide
Dosage Form
POWDER
Strength
100 g/100g
Labeler
Polypeptide Laboratories Inc
Marketing Category
BULK INGREDIENT
Substance
LINACLOTIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-04-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Teriparatide
Dosage Form
POWDER
Strength
100 g/100g
Labeler
Polypeptide Laboratories Inc
Marketing Category
BULK INGREDIENT
Substance
TERIPARATIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-11-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Teduglutide
Dosage Form
POWDER
Strength
100 g/100g
Labeler
Polypeptide Laboratories Inc
Marketing Category
BULK INGREDIENT
Substance
TEDUGLUTIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-04-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Gonadorelin Hydrochloride
Dosage Form
POWDER
Strength
125 g/125g
Labeler
Polypeptide Laboratories Inc
Marketing Category
BULK INGREDIENT
Substance
GONADORELIN ACETATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2020-11-16
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
LIRAGLUTIDE
Dosage Form
POWDER
Strength
1 g/g
Labeler
Polypeptide Laboratories Inc
Marketing Category
BULK INGREDIENT
Substance
LIRAGLUTIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
COSYNTROPIN
Dosage Form
POWDER
Strength
1 g/g
Labeler
Polypeptide Laboratories Inc
Marketing Category
BULK INGREDIENT
Substance
COSYNTROPIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
ETEPLIRSEN
Dosage Form
POWDER
Strength
1 g/g
Labeler
Polypeptide Laboratories Inc
Marketing Category
BULK INGREDIENT
Substance
ETEPLIRSEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-09-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Deslorelin
Dosage Form
POWDER
Strength
3 g/3g
Labeler
PolyPeptide Laboratories Private Limited
Marketing Category
BULK INGREDIENT
Substance
DESLORELIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-02-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Exenatide
Dosage Form
POWDER
Strength
250 g/250g
Labeler
PolyPeptide Laboratories Private Limited
Marketing Category
BULK INGREDIENT
Substance
EXENATIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-02-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Exenatide
Dosage Form
POWDER
Strength
1000 g/1000g
Labeler
PolyPeptide SA
Marketing Category
BULK INGREDIENT
Substance
EXENATIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2020-01-21
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Exenatide
Dosage Form
POWDER
Strength
1 g/g
Labeler
PolyPeptide SA
Marketing Category
BULK INGREDIENT
Substance
EXENATIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-05-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
SETMELANOTIDE ACETATE
Dosage Form
POWDER
Strength
1 g/g
Labeler
Polypeptide SA
Marketing Category
BULK INGREDIENT
Substance
SETMELANOTIDE ACETATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2020-11-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
ABALOPARATIDE
Dosage Form
POWDER
Strength
1 g/g
Labeler
Polypeptide SA
Marketing Category
BULK INGREDIENT
Substance
ABALOPARATIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-04-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Zilucoplan
Dosage Form
POWDER
Strength
150 g/150g
Labeler
Polypeptide SA
Marketing Category
BULK INGREDIENT
Substance
ZILUCOPLAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2025-02-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
SEMAGLUTIDE
Dosage Form
POWDER
Strength
1 g/g
Labeler
PolyPeptide SA
Marketing Category
BULK INGREDIENT
Substance
SEMAGLUTIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2020-06-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
NDC Type Breakdown
18 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).
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NDC
59162-0000
Nonproprietary Name
ZILUCOPLAN
Labeler
PolyPeptide Laboratories France
Dosage Form
POWDER
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