Bepotastine Besilate - NDC Database

NDC Database
4 labelers

Bepotastine Besilate

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

BULK INGREDIENT
Last Marketing Date
2014-02-27
Data Source
FDA
First Marketing Date
2009-08-20
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NDC Records Timeline (4 records)
Clear
2011
01 Nov
Icrom S.r.l.
BULK INGREDIENT

NDC

40700-0040

Labeler

Icrom S.r.l.

Nonproprietary Name

Bepotastine Besilate

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 g/g

Start Marketing: 2011-11-01

Substance

BEPOTASTINE BESILATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-11-01

End Marketing Date

-

Listing / Certification

2026-12-31

2009
20 Aug
UBE Corporation
BULK INGREDIENT

NDC

42672-0100

Labeler

UBE Corporation

Nonproprietary Name

Bepotastine

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2009-08-20

Substance

BEPOTASTINE BESILATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-08-20

End Marketing Date

-

Listing / Certification

2026-12-31

2013
16 Aug
BULK INGREDIENT

NDC

42571-277

Labeler

Micro Labs Limited

Nonproprietary Name

Bepotastine Besilate

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

10 kg/10kg

Start Marketing: 2013-08-16

Substance

BEPOTASTINE BESILATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2013-08-16

End Marketing Date

-

Listing / Certification

2026-12-31

2014
27 Feb
BULK INGREDIENT

NDC

14501-0088

Labeler

MSN Laboratories Private Limited

Nonproprietary Name

Bepotastine Besilate

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2014-02-27

Substance

BEPOTASTINE BESILATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-02-27

End Marketing Date

-

Listing / Certification

2026-12-31

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Product Type Breakdown
4 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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Substance

BEPOTASTINE BESILATE

Identifiers

NDC: 40700-0040
DEA Schedule:

Official FDA Data

Based on publicly available FDA NDC information

National Drug Code

Structured NDC product information

Product Information

Drug, labeler and marketing data

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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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