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Gramicidin D

Generic Name
Gramicidin D
Brand Names
Sofracort, Soframycin, Triple Antibiotic, Viaderm Kc
Drug Type
Small Molecule
Chemical Formula
C96H135N19O16
CAS Number
1405-97-6
Unique Ingredient Identifier
5IE62321P4

Overview

Gramcidin D is a heterogeneous mixture of three antibiotic compounds, gramicidins A, B and C, making up 80%, 6%, and 14% respectively all of which are obtained from the soil bacterial species Bacillus brevis and called collectively gramicidin D. Gramcidins are 15 residue peptides with alternating D and L amino acids, which assemble inside of the hydrophobic interior of the cellular lipid bilayer to form a β-helix. Active against most Gram-positive bacteria and some Gram-negative organisms, Gramicidin D is used primarily as a topical antibiotic and is also found in Polysporin ophthalmic solution.

Indication

For treatment of skin lesions, surface wounds and eye infections.

Associated Conditions

  • Allergic Conjunctivitis (AC)
  • Allergic Skin Reaction
  • Blepharoconjunctivitis
  • Conjunctivitis
  • Conjunctivitis infective
  • Episcleritis
  • External ear inflammation
  • Eye and eyelid infections
  • Inflammatory Skin Disease
  • Iridocyclitis
  • Keratitis
  • Ocular Inflammation
  • Otitis Externa
  • Rosacea conjunctivitis
  • Scleritis
  • Seborrhoea of the External Ear
  • Stye
  • Ulcerative keratitis
  • Bacterial blepharitis
  • Infected eczema of the Eyelid
  • Superficial ocular infections

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor

No clinical trials found

No clinical trials found for this drug

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
A-S Medication Solutions
50090-0247
OPHTHALMIC
0.025 mg in 1 mL
8/2/2022
Dispensing Solutions, Inc.
55045-1194
OPHTHALMIC
0.025 mg in 1 mL
11/7/2011
Bausch & Lomb Incorporated
24208-790
OPHTHALMIC
0.025 mg in 1 mL
8/2/2022
Physicians Total Care, Inc.
54868-6253
OPHTHALMIC
0.025 mg in 1 mL
5/4/2011
Rebel Distributors Corp
21695-528
OPHTHALMIC
0.025 mg in 1 mL
2/22/2007

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
No HSA approvals found for this drug.

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
SWISSCORT CREAM
N/A
N/A
N/A
8/31/1982

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
LIDOSPORIN CREAM
warner-lambert canada inc.
02230842
Cream - Topical
0.25 MG / G
7/8/1998
LIDOSPORIN CREAM
glaxo wellcome inc.
01966006
Cream - Topical
0.25 MG / G
12/31/1971
ANTIBIOTIC CREAM
cellchem pharmaceuticals inc.
02311844
Cream - Topical
0.25 MG / G
12/23/2009
TRIPLE ANTIBIOTIC OINTMENT
cellchem pharmaceuticals inc.
02297949
Ointment - Topical
0.25 MG / G
12/23/2009
POLYSPORIN EYE AND EAR DROPS STERILE
johnson & johnson inc
02239156
Drops - Otic ,  Ophthalmic
0.025 MG / ML
2/12/2000
OPTIMYXIN PLUS
euro-pharm international canada inc
00807435
Solution - Ophthalmic ,  Otic
0.025 MG / ML
12/31/1989
SANDOZ OPTICORT
02247920
Solution - Otic ,  Ophthalmic
0.05 MG / ML
1/16/2004
TEVA-TRIACOMB
teva canada limited
00550507
Cream - Topical
0.25 MG / G
12/31/1992
TRIPLE ANTIBIOTIC OINTMENT
melaleuca of canada inc.
02088339
Ointment - Topical
.25 MG / G
12/31/1994
SOFRACORT STERILE EAR/EYE DROPS
hoechst roussel canada inc.
01987712
Drops - Topical
0.05 MG / ML
12/31/1966

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
OFTALMOWELL COLIRIO EN SOLUCIÓN
Teofarma S.R.L.
45030
COLIRIO EN SOLUCIÓN
Medicamento Sujeto A Prescripción Médica
Commercialized
MIDACINA POMADA
Laboratorio De Especialidades Nacionales S.A.
53744
POMADA
Medicamento Sujeto A Prescripción Médica
Commercialized
FLODERMOL POMADA
Laboratorios Ern S.A.
48394
POMADA
Medicamento Sujeto A Prescripción Médica
Not Commercialized

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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