Overview
Zea mays pollen is the pollen of the Zea mays plant. Zea mays pollen is mainly 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 |
|---|---|---|---|---|---|
| Antigen Laboratories, Inc. | 49288-0657 | SUBCUTANEOUS, INTRADERMAL | 0.000227 g in 1 mL | 12/2/2009 | |
| Nelco Laboratories, Inc. | 36987-2309 | INTRADERMAL, SUBCUTANEOUS | 0.05 g in 1 mL | 12/4/2009 | |
| Antigen Laboratories, Inc. | 49288-0141 | SUBCUTANEOUS, INTRADERMAL | 0.05 g in 1 mL | 11/13/2009 | |
| Allergy Laboratories, Inc. | 54575-091 | PERCUTANEOUS, SUBCUTANEOUS | 1 g in 20 mL | 3/15/2011 | |
| Nelco Laboratories, Inc. | 36987-2303 | INTRADERMAL, SUBCUTANEOUS | 10000 [PNU] in 1 mL | 12/4/2009 | |
| Nelco Laboratories, Inc. | 36987-2304 | INTRADERMAL, SUBCUTANEOUS | 10000 [PNU] in 1 mL | 12/4/2009 | |
| Nelco Laboratories, Inc. | 36987-2308 | INTRADERMAL, SUBCUTANEOUS | 0.05 g in 1 mL | 12/4/2009 | |
| Nelco Laboratories, Inc. | 36987-2310 | INTRADERMAL, SUBCUTANEOUS | 0.1 g in 1 mL | 12/4/2009 | |
| Nelco Laboratories, Inc. | 36987-2307 | INTRADERMAL, SUBCUTANEOUS | 40000 [PNU] in 1 mL | 12/4/2009 | |
| Nelco Laboratories, Inc. | 36987-2305 | INTRADERMAL, SUBCUTANEOUS | 20000 [PNU] in 1 mL | 12/4/2009 |
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 |
|---|---|---|---|---|---|
| UT Cleanse | 427926 | Medicine | A | 11/15/2023 | |
| Ultimé Men's Prostate Support | 401470 | Medicine | A | 12/21/2022 | |
| Ultimé Urinary Tract Support | 391038 | Medicine | A | 6/21/2022 | |
| METAGENICS KIDNEY CARE | 394051 | Medicine | A | 8/18/2022 | |
| SLEEP | 440311 | Vida Glow Pty Ltd | Medicine | A | 2/8/2024 |
| Cell-u-loss | 311351 | Medicine | A | 11/9/2018 | |
| YANG YIN JIANG YA WAN | 218861 | Medicine | A | 1/2/2014 | |
| YANG YIN JIANG YA FANG | 177402 | Medicine | A | 11/8/2010 | |
| ageLOC Y-Span | 339998 | Medicine | A | 7/23/2020 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
|---|---|---|---|---|---|
| URINATONE BALSAM | thuna herbal remedies ltd. | 00462799 | Liquid - Oral | 388 MG / 30 ML | 12/31/1947 |
| DIUROL CAP | gahler enterprises ltd. | 00899720 | Capsule - Oral | 100 MG / CAP | 12/31/1991 |
| STIGMATA MAYDIS-INJEEL LIQ | 02065088 | Liquid - Oral | 10 D / 1.1 ML | 12/31/1994 | |
| NO. 1 URATONE TEA | 3 way herbs ltd. | 02025140 | Tea (Herbal) - Oral | 136 MG / 5 ML | 12/31/1993 |
| #17 DIURETIC TEA | 3 way herbs ltd. | 02008580 | Tea (Herbal) - Oral | 136 MG / 5 ML | 12/31/1993 |
| STIGMATA MAIDIS | total health centre | 02236314 | Drops - Oral | 1 X | 4/1/1998 |
| STIGMATA MAIDIS GRAN (1CH-30CH) | homeocan inc. | 01953478 | Tablet - Oral | 1 CH / TAB | 12/31/1991 |
| UNDA 38 | seroyal international inc. | 02233257 | Pellet
,
Tablet
,
Granules
,
Drops
,
Liquid - Oral | 4 X | 4/6/1998 |
| STIGMATA MAYDIS-INJEEL FORTE LIQ (4D,10D,30D,200D/1.1ML) | 02065061 | Liquid - Oral | 4 D / 1.1 ML | 12/31/1994 | |
| DIURETIC TABLETS | thuna herbal remedies ltd. | 00646083 | Tablet - Oral | 147 MG | 12/31/1985 |
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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