Digitalis pupurea is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Washington Homeopathic Products. The primary component is Digitalis.
Product ID | 68428-357_6d350c70-6437-3c93-e053-2991aa0acd1d |
NDC | 68428-357 |
Product Type | Human Otc Drug |
Proprietary Name | Digitalis pupurea |
Generic Name | Digitalis |
Dosage Form | Pellet |
Route of Administration | ORAL |
Marketing Start Date | 2010-02-03 |
Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
Labeler Name | Washington Homeopathic Products |
Substance Name | DIGITALIS |
Active Ingredient Strength | 30 [hp_C]/1 |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2010-02-03 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-02-03 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-02-03 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-02-03 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-02-03 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-02-03 |
Ingredient | Strength |
---|---|
DIGITALIS | 30 [hp_C]/1 |
SPL SET ID: | 5b1601ed-aa4a-4ff4-a9d4-2caa5ff1e312 |
Manufacturer | |
UNII | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
68428-357 | Digitalis pupurea | DIGITALIS |
0220-1756 | Digitalis purpurea | DIGITALIS |
0220-1757 | Digitalis purpurea | DIGITALIS |
0220-1761 | Digitalis purpurea | DIGITALIS |
0220-1764 | Digitalis purpurea | DIGITALIS |
0220-1767 | Digitalis purpurea | DIGITALIS |
71919-256 | Digitalis purpurea | DIGITALIS |
68428-141 | Digitalis Purpurea Kit Refill | DIGITALIS |
64117-139 | Nausea Headache | DIGITALIS |