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HA
HA - 57520-0105-1 - (Belladonna, Bryonia alba, Gelsemium sempervirens, Glonoinum, Melilotus officinalis,)
Drug Information of HA
| Product NDC: | 57520-0105 |
| Proprietary Name: | HA |
| Non Proprietary Name: | Belladonna, Bryonia alba, Gelsemium sempervirens, Glonoinum, Melilotus officinalis, |
| Active Ingredient(s): | 30; 30; 30; 30; 30; 30; 30; 30; 30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp; Belladonna, Bryonia alba, Gelsemium sempervirens, Glonoinum, Melilotus officinalis, |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of HA
| Product NDC: | 57520-0105 |
| Labeler Name: | Apotheca Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20100218 |
Package Information of HA
| Package NDC: | 57520-0105-1 |
| Package Description: | 30 mL in 1 BOTTLE, DROPPER (57520-0105-1) |
NDC Information of HA
| NDC Code | 57520-0105-1 |
| Proprietary Name | HA |
| Package Description | 30 mL in 1 BOTTLE, DROPPER (57520-0105-1) |
| Product NDC | 57520-0105 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Belladonna, Bryonia alba, Gelsemium sempervirens, Glonoinum, Melilotus officinalis, |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20100218 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Apotheca Company |
| Substance Name | ATROPA BELLADONNA; BRYONIA ALBA ROOT; GELSEMIUM SEMPERVIRENS ROOT; MELILOTUS OFFICINALIS POLLEN; NITROGLYCERIN; SILICON DIOXIDE; SODIUM CHLORIDE; SPIGELIA; STRYCHNOS NUX-VOMICA SEED |
| Strength Number | 30; 30; 30; 30; 30; 30; 30; 30; 30 |
| Strength Unit | [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
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