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Dicyclomaine manufacturers

73 products found

Filters

73 products found

dicyclomaine + mefenamic acid

Tablets 10 mg + 250 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
India
Manufacturer #21247

Manufacturer usually replies in 3 days

dicyclomaine

Tablets 20 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #20084

Manufacturer usually replies in 1 days

dicyclomaine

Tablets 20 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #20084

Manufacturer usually replies in 1 days

dicyclomaine + diclofenac sodium

Capsules 50 mg + 50 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #18174

Manufacturer usually replies in 4 days

dicyclomaine + mefenamic acid

Tablets 10 mg + 250 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #18174

Manufacturer usually replies in 4 days

dicyclomaine + paracetamol + diclofenac sodium

Tablets 20 mg + 325 mg + 50 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #17478

Manufacturer usually replies in 1 days

dicyclomaine + aluminium hydroxide + magnesium hydroxide

Oral suspension 2.5 mg + 200 mg + 100 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #20395

Manufacturer usually replies in 9 days

dicyclomaine + paracetamol

Tablets 20 mg + 500 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #20290

Manufacturer usually replies in 8 days

dicyclomaine + nimesulide

Tablets 10 mg + 100 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #20087

Manufacturer usually replies in 8 days

dicyclomaine + paracetamol

Tablets 20 mg + 500 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #18474

Manufacturer usually replies in 9 days

dicyclomaine + simethicone

Oral suspension 10 mg + 40 mg / 5 ml

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #18461

Manufacturer usually replies in 8 days

dicyclomaine + dimethicone

Oral drops 10 mg + 40 mg / ml / 5 ml

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #17808

Manufacturer usually replies in 14 days

dicyclomaine + paracetamol

Tablets 20 mg + 325 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #20499

Manufacturer usually replies in 75 days

dicyclomaine + simethicone

Oral suspension 10 mg + 40 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #20509

dicyclomaine + paracetamol

Oral suspension 50 mg + 125 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #20509

dicyclomaine + mefenamic acid

Tablets for oral solution 10 mg + 250 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #19779

dicyclomaine + paracetamol + simethicone

Tablets 20 mg + 650 mg + 50 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #18232

dicyclomaine + paracetamol

Tablets 20 mg + 325 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #17641

dicyclomaine

Tablets 10 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
Taiwan
GMP approvals
PICS
Manufacturer #20552
The company was established in the 1950s, quality is the main focus of continuous quality improvement programs and extensive efforts to pursue perfection. Throughout the half-century, recognition has been gained from multinational companies all over the world. The company follows straight of the PIC/S GMP standard, starting from raw material quality inspection, and in-process quality control to end product quality assurance, complete sets of quality records are kept for analysis and future reference.

Manufacturer usually replies in nan days

dicyclomaine

Injection 10 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
Taiwan
GMP approvals
PICS
Manufacturer #20552
The company was established in the 1950s, quality is the main focus of continuous quality improvement programs and extensive efforts to pursue perfection. Throughout the half-century, recognition has been gained from multinational companies all over the world. The company follows straight of the PIC/S GMP standard, starting from raw material quality inspection, and in-process quality control to end product quality assurance, complete sets of quality records are kept for analysis and future reference.

Manufacturer usually replies in nan days

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