NDC 15631-0014
ALFALFA
Alfalfa
ALFALFA is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Alfalfa.
| Product ID | 15631-0014_9e3858bc-97fa-62e4-e053-2995a90a58c1 |
| NDC | 15631-0014 |
| Product Type | Human Otc Drug |
| Proprietary Name | ALFALFA |
| Generic Name | Alfalfa |
| Dosage Form | Pellet |
| Route of Administration | ORAL |
| Marketing Start Date | 2015-10-02 |
| Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
| Labeler Name | Rxhomeo Private Limited d.b.a. Rxhomeo, Inc |
| Substance Name | ALFALFA |
| Active Ingredient Strength | 1 [hp_X]/1 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |
Packaging
NDC 15631-0014-0
100 PELLET in 1 PACKAGE (15631-0014-0)
| Marketing Start Date | 2018-01-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 15631-0014-4 [15631001404]
ALFALFA PELLET
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-01 |
| Inactivation Date | 2020-01-31 |
| Reactivation Date | 2020-02-10 |
NDC 15631-0014-5 [15631001405]
ALFALFA PELLET
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-01 |
| Inactivation Date | 2020-01-31 |
| Reactivation Date | 2020-02-10 |
NDC 15631-0014-0 [15631001400]
ALFALFA PELLET
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-01 |
| Inactivation Date | 2020-01-31 |
| Reactivation Date | 2020-02-10 |
NDC 15631-0014-2 [15631001402]
ALFALFA PELLET
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-01 |
| Inactivation Date | 2020-01-31 |
| Reactivation Date | 2020-02-10 |
NDC 15631-0014-3 [15631001403]
ALFALFA PELLET
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-01 |
| Inactivation Date | 2020-01-31 |
| Reactivation Date | 2020-02-10 |
NDC 15631-0014-1 [15631001401]
ALFALFA PELLET
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-01 |
| Inactivation Date | 2020-01-31 |
| Reactivation Date | 2020-02-10 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| ALFALFA | 1 [hp_X]/1 |
OpenFDA Data
| SPL SET ID: | 42a7150b-5497-41aa-b7a3-8184bc15b392 |
| Manufacturer | |
| UNII |
NDC Crossover Matching brand name "ALFALFA" or generic name "Alfalfa"
| 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 |
Trademark Results [ALFALFA]
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