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
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2024/01/17 | Phase 1 | Recruiting | |||
2011/09/26 | Phase 1 | Completed |
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 |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
BENADRYL ORIGINAL oral liquid bottle (reformulation) | 199371 | Medicine | A | 7/16/2012 | |
CODRAL DRY COUGH & COLD WITH ANTIHISTAMINE oral liquid bottle | 347350 | Medicine | A | 11/4/2020 | |
NYAL BRONCHITIS COUGH MEDICINE ammonium chloride 11mg/mL oral liquid bottle | 13654 | Medicine | A | 9/10/1991 | |
CHEMISTS' OWN DIFENACOL cough mixture oral liquid bottle | 10977 | Medicine | A | 8/13/1991 |
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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