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List of NDC API details of 012C11ZU6G Active Pharmaceutical Ingredient listed on PharmaCompass.com

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SERVICES
Flag India
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Terbinafine Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
55111-024
2002-03-06
2024-12-31
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Terbinafine Hydrochloride
POWDER (50kg/50kg)
BULK INGREDIENT
65862-364
2023-11-15
2024-12-31
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Terbinafine hydrochloride
POWDER (1g/g)
BULK INGREDIENT FOR ...
73309-177
2020-08-10
2023-12-31
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Terbinafine Hydrochloride
POWDER (25kg/25kg)
BULK INGREDIENT
66219-0001
2009-12-04
2024-12-31
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TERBINAFINE HYDROCHLORIDE
POWDER (1kg/kg)
BULK INGREDIENT
52562-600
2011-09-21
2024-12-31
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Terbinafine Hydrochloride
POWDER (25kg/25kg)
BULK INGREDIENT
53104-7577
2016-01-01
2024-12-31
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Terbinafine HCl
POWDER (1g/g)
BULK INGREDIENT
71052-010
2017-07-01
2024-12-31
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Terbinafine Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
59349-0037
2023-03-03
2024-12-31
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Terbinafine Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
59349-0007
2008-12-29
2024-12-31
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Terbinafine Hydrochloride
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59349-0038
2023-03-03
2024-12-31
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TERBINAFINE HYDROCHLORIDE
POWDER (1kg/kg)
BULK INGREDIENT
48087-0079
2010-04-12
2024-12-31
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Terbinafine HCl
POWDER (1g/g)
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51552-1451
2015-11-01
2024-06-30
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Terbinafine HCl
POWDER (1g/g)
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51552-1422
2019-12-04
2024-12-31
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Terbinafine Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
66039-817
2005-03-14
2024-12-31
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Terbinafine Hydrochloride
POWDER (1kg/kg)
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66039-859
2008-01-11
2024-12-31
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Terbinafine Hydrochloride
POWDER (1kg/kg)
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68554-0002
1992-12-30
2024-12-31
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Terbinafine Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
69037-0049
1996-05-10
2025-12-31
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TERBINAFINE HCL
POWDER (1g/g)
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60592-023
2020-01-09
2024-12-31
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Terbinafine Hydrochloride
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62991-3085
2015-05-14
2024-12-31
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Terbinafine Hydrochloride
POWDER (1g/g)
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38779-3253
2022-01-27
2024-12-31
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Terbinafine Hydrochloride
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38779-2481
2009-07-14
2024-12-31
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Terbinafine Hydrochloride
POWDER (1kg/kg)
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14501-0012
2010-03-25
2024-12-31
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TERBINAFINE HYDROCHLORIDE
POWDER (1kg/kg)
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51927-4856
2014-12-12
2024-12-31
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Terbinafine Hydrochloride
POWDER (1kg/kg)
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53069-0530
2004-12-14
2024-12-31
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Terbinafine Hydrochloride
POWDER (1kg/kg)
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49386-007
2013-05-03
2024-12-31
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Terbinafine Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
52286-0007
2009-11-04
2024-12-31
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TERBINAFINE HYDROCHLORIDE
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70159-006
2017-09-12
2024-12-31
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  • TABLET;ORAL - EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • CREAM;TOPICAL - 1%
  • SOLUTION;TOPICAL - 1%
  • GRANULE;ORAL - EQ 125MG BASE/PACKET
  • GRANULE;ORAL - EQ 187.5MG BASE/PACKET

Looking for 78628-80-5 / Terbinafine Hydrochloride API manufacturers, exporters & distributors?

Terbinafine Hydrochloride manufacturers, exporters & distributors 1

80

PharmaCompass offers a list of Terbinafine Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Terbinafine Hydrochloride manufacturer or Terbinafine Hydrochloride supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Terbinafine Hydrochloride manufacturer or Terbinafine Hydrochloride supplier.

PharmaCompass also assists you with knowing the Terbinafine Hydrochloride API Price utilized in the formulation of products. Terbinafine Hydrochloride API Price is not always fixed or binding as the Terbinafine Hydrochloride Price is obtained through a variety of data sources. The Terbinafine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Terbinafine Hydrochloride

Synonyms

Terbinafine hcl, 78628-80-5, Lamisil at, (e)-n,6,6-trimethyl-n-(naphthalen-1-ylmethyl)hept-2-en-4-yn-1-amine hydrochloride, Bramazil, Bramizil

Cas Number

78628-80-5

Unique Ingredient Identifier (UNII)

012C11ZU6G

About Terbinafine Hydrochloride

A naphthalene derivative that inhibits fungal SQUALENE EPOXIDASE and is used to treat DERMATOMYCOSES of the skin and nails.

012C11ZU6G Manufacturers

A 012C11ZU6G manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 012C11ZU6G, including repackagers and relabelers. The FDA regulates 012C11ZU6G manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 012C11ZU6G API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

click here to find a list of 012C11ZU6G manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

012C11ZU6G Suppliers

A 012C11ZU6G supplier is an individual or a company that provides 012C11ZU6G active pharmaceutical ingredient (API) or 012C11ZU6G finished formulations upon request. The 012C11ZU6G suppliers may include 012C11ZU6G API manufacturers, exporters, distributors and traders.

click here to find a list of 012C11ZU6G suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

012C11ZU6G NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing 012C11ZU6G as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for 012C11ZU6G API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture 012C11ZU6G as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain 012C11ZU6G and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a 012C11ZU6G NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of 012C11ZU6G suppliers with NDC on PharmaCompass.

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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