Overview
Parsley allergenic extract is used in allergenic testing.
Indication
No indication information available.
Associated Conditions
No associated conditions information available.
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 |
---|---|---|---|---|---|
Nelco Laboratories, Inc. | 36987-1481 | INTRADERMAL, SUBCUTANEOUS | 0.1 g in 1 mL | 12/9/2009 | |
Antigen Laboratories, Inc. | 49288-0377 | SUBCUTANEOUS, INTRADERMAL | 0.05 g in 1 mL | 11/17/2009 | |
Nelco Laboratories, Inc. | 36987-1480 | INTRADERMAL, SUBCUTANEOUS | 0.1 g in 1 mL | 12/9/2009 | |
Nelco Laboratories, Inc. | 36987-1479 | INTRADERMAL, SUBCUTANEOUS | 0.05 g in 1 mL | 12/9/2009 | |
Nelco Laboratories, Inc. | 36987-1478 | INTRADERMAL, SUBCUTANEOUS | 0.05 g in 1 mL | 12/9/2009 | |
Allergy Laboratories, Inc. | 54575-428 | PERCUTANEOUS, SUBCUTANEOUS | 1 g in 20 mL | 3/15/2011 |
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 |
---|---|---|---|---|---|
No PPB approvals found for this drug. |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
MY-LIFE CORPORATION BIOGEN IMPROVED oral powder jar (export) | 52453 | Worrell Whitehill (Liquidator For Mylife Corp Pty Ltd) | Medicine | A | 5/9/1995 |
OZWAY INTERNATIONAL BCN oral powder jar | 55785 | Ozway Natural Products | Medicine | A | 5/30/1996 |
Young Living Olive Essentials | 326006 | Medicine | A | 11/7/2019 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
---|---|---|---|---|---|
RENTOX | bio active canada ltd. | 02233676 | Liquid - Oral | 3 X | 1/19/1998 |
PETROSELINUM-INJEEL LIQ (12D,30D,200D/1.1ML) | 02062747 | Liquid - Oral | 12 D / 1.1 ML | 12/31/1994 | |
LIVER AND KIDNEY TEA THUNAS | thuna herbal remedies ltd. | 00190446 | Tea (Herbal) - Oral | 3.97 G / 30 G | 6/11/1980 |
GALL BLADDER FORMULA BLACKHAWKS | blackhawk indian remedy co | 00221260 | Tablet - Oral | 25 MG | 12/31/1969 |
DANDIPLEX | bio active canada ltd. | 02233595 | Liquid - Oral | 1 X | 5/26/1998 |
BAYBERRYPLEX | bio active canada ltd. | 02233592 | Liquid - Oral | 1 X | 5/26/1998 |
HDR I | bio active canada ltd. | 02233622 | Liquid - Oral | 1 X | 5/26/1998 |
PETROSELINUM SATIVUM | dolisos canada inc. | 02234659 | Liquid
,
Globules
,
Granules - Oral | 1 X | 1/5/1998 |
HERBAL DIURETIC - TABLETS | quest vitamins a div of purity life health products | 02153122 | Tablet - Oral | 40 MG / TAB | 12/31/1995 |
HKI DPS | seroyal international inc. | 00729108 | Drops - Oral | 6 X / X | 12/31/1988 |
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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