Alfalfa is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Washington Homeopathic Products. The primary component is Alfalfa.
Product ID | 71919-027_7e3e06c4-b054-5d77-e053-2991aa0a7cec |
NDC | 71919-027 |
Product Type | Human Otc Drug |
Proprietary Name | Alfalfa |
Generic Name | Alfalfa |
Dosage Form | Liquid |
Route of Administration | ORAL |
Marketing Start Date | 2011-05-17 |
Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
Labeler Name | Washington Homeopathic Products |
Substance Name | ALFALFA |
Active Ingredient Strength | 30 [hp_C]/mL |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2011-05-17 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2011-05-17 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2011-05-17 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2011-05-17 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2011-05-17 |
Ingredient | Strength |
---|---|
ALFALFA | 30 [hp_C]/mL |
SPL SET ID: | 8af1f4cc-6333-455d-b9d1-445815a2a93d |
Manufacturer | |
UNII | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
0220-0161 | Alfalfa | ALFALFA |
0220-0164 | Alfalfa | ALFALFA |
15631-0014 | ALFALFA | ALFALFA |
15631-0507 | ALFALFA | ALFALFA |
22840-1507 | Alfalfa | Medicago sativa |
22840-1508 | Alfalfa | Medicago sativa |
22840-1509 | Alfalfa | Medicago sativa |
22840-1561 | Alfalfa | Medicago sativa |
22840-5503 | Alfalfa | Medicago sativa |
60512-6469 | ALFALFA | ALFALFA |
68428-872 | Alfalfa | ALFALFA |
71919-027 | Alfalfa | ALFALFA |
0268-1012 | MEDICAGO SATIVA POLLEN | Alfalfa |
0268-1013 | MEDICAGO SATIVA POLLEN | Alfalfa |
0268-6602 | MEDICAGO SATIVA POLLEN | Alfalfa |