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Ammonium chloride

Generic Name
Ammonium chloride
Brand Names
Damylin With Codeine
Drug Type
Small Molecule
Chemical Formula
ClH4N
CAS Number
12125-02-9
Unique Ingredient Identifier
01Q9PC255D

Overview

Ammonium chloride is an inorganic compound with the formula NH4Cl. It is highly soluble in water producing mildly acidic solutions.

Indication

1.干咳以及痰不易咳出等;2.酸化尿液;3.纠正重度代谢性碱中毒,应用足量氯化钠注射液不能满意纠正者;4.氯化铵负荷试验可了解肾小管酸化功能,用于肾小管性酸中毒的鉴别诊断。

Associated Conditions

  • Allergic Reaction
  • Allergic cough
  • Common Cold
  • Cough
  • Cough caused by Common Cold
  • Diabetes
  • Hypertension
  • Metabolic Alkalosis
  • Nasal Congestion
  • Nasal Congestion Due to Allergic Rhinitis
  • Productive cough
  • Rhinorrhoea
  • Sneezing
  • Bronchial congestion
  • Dry cough
  • Excess mucus or phlegm
  • Hypochloremic state

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
King Bio Inc.
57955-6031
ORAL
10 [hp_X] in 59 mL
5/23/2025
Deseret Biologicals, Inc.
43742-2244
ORAL
6 [hp_X] in 1 mL
5/27/2025
Apotheca Company
57520-0228
ORAL
200 [hp_X] in 1 mL
6/9/2025

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
PHENEXPECT SYRUP
SIN09014P
SYRUP
135 mg/5 ml
11/28/1996
DIPHEN 10 EXPECTORANT
SIN08799P
SYRUP
125 mg/5 ml
7/3/1996
SUNTUSS SYRUP
SIN03491P
SYRUP
125 mg/5 ml
6/24/1989
UNIDRYL CD EXPECTORANT
SIN02917P
SYRUP
135mg/5ml
5/22/1989
PHENEXPECT CD SYRUP
SIN06702P
SYRUP
135 mg/5 ml
12/3/1991
POLINS COUGH MIXTURE (REVISED FORMULA)
SIN09473P
SOLUTION
80 mg/5 ml
8/19/1997
DEXCOPHAN COUGH LINCTUS PLUS
SIN07643P
ELIXIR
150 mg/5 ml
2/8/1994
BRECOLIN COUGH MIXTURE
SIN04972P
SOLUTION
100 mg/5 ml
7/25/1990
DIPHEN 5 EXPECTORANT
SIN08782P
SYRUP
62.5 mg/5 ml
7/3/1996
XSP-BENA EXPECTORANT
SIN03335P
SUSPENSION
135 mg/5 ml
6/16/1989

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
DIPHENMIN EXPECTORANT
N/A
N/A
N/A
4/27/1979
PACTOREX SYRUP
N/A
N/A
N/A
4/20/1979
U-BANOL "S" EXPECTORANT
N/A
synco (h.k.) limited
N/A
N/A
4/20/1979
SENEX COUGH SYRUP
N/A
N/A
N/A
2/3/1999
THENADYL E C COMPOUND SYRUP
N/A
N/A
N/A
5/3/1979
FUTALO COUGH SYRUP
N/A
N/A
N/A
8/21/1989
PHECOBO COUGH SYRUP
N/A
N/A
N/A
7/3/1998
UNI-RAMINE D.E. SYRUP
N/A
N/A
N/A
7/3/1998
HONEY CHILD COUGH SYRUP
N/A
N/A
N/A
12/7/2009
GUSILON COUGH LINCTUS
N/A
karen laboratories o/b karen pharmaceutical co ltd
N/A
N/A
5/17/1982

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
FORMULA 22158
therapeutic foods co.
00191531
Capsule - Oral
7 MG / CAP
5/18/1994
BRONCHIAL COUGH SYR
theralab inc.
00525499
Syrup - Oral
45 MG / ML
12/31/1981
BRONCH EZE
pharmavite laboratories (1987) inc.
00484709
Syrup - Oral
100 MG / 5 ML
12/31/1984
AMMONIUM MURIATICUM GOUTTE 1CH - 30CH
boiron laboratoires
00686611
Drops - Oral
1 CH / CH
12/31/1987
AMBENYL COUGH SYRUP
parke-davis division, warner-lambert canada inc.
00469122
Liquid - Oral
80 MG / 5 ML
12/31/1979
SUPPRESS COUGH SYR W.COD.DIPHEN.HCL AMM.CHL.
stanley pharmaceuticals, a division of vita health products inc.
02190575
Syrup - Oral
125 MG / 5 ML
12/31/1996
DM PLUS COUGH SYRUP
technilab pharma inc.
02097346
Syrup - Oral
125 MG / 5 ML
12/31/1995
AMMONIUM MURIATICUM LIQUID (S NO. 33)
total health centre
02180340
Liquid - Oral
1 X / ML
6/1/1997
COUGH SYR W CODEINE DIPHENHYD HCL & AMMON CL
stanley pharmaceuticals, a division of vita health products inc.
00792160
Syrup - Oral
125 MG / 5 ML
12/31/1989
COUGH AND ALLERGY SYRUP WITH CODEINE
laboratoire riva inc.
02486903
Syrup - Oral
125 MG / 5 ML
10/8/2019

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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