DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr.Reddy's Laboratories Limited
02 1Aurobindo Pharma Limited
03 1Changzhou Tianhua Pharmaceutical Co., Ltd.
04 1Chromo Laboratories India Private Limited
05 1Cipla Ltd.
06 1Darmerica, LLC
07 2Derivados Quimicos
08 1Derivados Quimicos SAU
09 1F.I.S. FABBRICA ITALIANA SINTETICI S.P.A.
10 2Glenmark Life Sciences Limited
11 1Hetero Labs Limited
12 1Honour Lab Limited
13 1Kalchem International inc
14 1LETCO MEDICAL, LLC
15 1MSN Laboratories Private Limited
16 1Medisca Inc,
17 1Medisca Inc.
18 1Professional Compounding Centers of America dba PCCA
19 1Quimica Sintetica S.A.
20 1Shandong Anhong Pharmaceutical Co., Ltd.
21 1UQUIFA Mexico, S.A. DE C.V.
22 1Vijayasri Organics Private Limited
01 1TERBINAFINE HCL
02 4TERBINAFINE HYDROCHLORIDE
03 1Terbinafine HCl
04 18Terbinafine Hydrochloride
01 2China
02 10India
03 1Italy
04 5Spain
05 5U.S.A
06 1United Kingdom
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-024
Start Marketing Date : 2002-03-06
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52562-600
Start Marketing Date : 2011-09-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48087-0079
Start Marketing Date : 2010-04-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-3253
Start Marketing Date : 2022-01-27
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-2481
Start Marketing Date : 2009-07-14
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 14501-0012
Start Marketing Date : 2010-03-25
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-4856
Start Marketing Date : 2014-12-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 53069-0530
Start Marketing Date : 2004-12-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49386-007
Start Marketing Date : 2013-05-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52286-0007
Start Marketing Date : 2009-11-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Terbinafine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Terbinafine Hydrochloride, including repackagers and relabelers. The FDA regulates Terbinafine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Terbinafine Hydrochloride 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 Terbinafine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Terbinafine Hydrochloride supplier is an individual or a company that provides Terbinafine Hydrochloride active pharmaceutical ingredient (API) or Terbinafine Hydrochloride finished formulations upon request. The Terbinafine Hydrochloride suppliers may include Terbinafine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Terbinafine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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 Terbinafine Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Terbinafine Hydrochloride API and other APIs are published in this directory by the FDA.
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 Terbinafine Hydrochloride 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.
The NDC directory also contains data on finished compounded human drug products that contain Terbinafine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Terbinafine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Terbinafine Hydrochloride suppliers with NDC on PharmaCompass.
We have 20 companies offering Terbinafine Hydrochloride
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