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Cocculus compositum
Cocculus compositum - 50114-6045-2 - (ANAMIRTA COCCULUS SEED and CONIUM MACULATUM FLOWERING TOP and AMBERGRIS)
Drug Information of Cocculus compositum
| Product NDC: | 50114-6045 |
| Proprietary Name: | Cocculus compositum |
| Non Proprietary Name: | ANAMIRTA COCCULUS SEED and CONIUM MACULATUM FLOWERING TOP and AMBERGRIS |
| Active Ingredient(s): | 6; 4; 3 [hp_X]/1; [hp_X]/1; [hp_X]/1 & nbsp; ANAMIRTA COCCULUS SEED and CONIUM MACULATUM FLOWERING TOP and AMBERGRIS |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cocculus compositum
| Product NDC: | 50114-6045 |
| Labeler Name: | Heel Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 19840131 |
Package Information of Cocculus compositum
| Package NDC: | 50114-6045-2 |
| Package Description: | 100 TABLET in 1 BOTTLE (50114-6045-2) |
NDC Information of Cocculus compositum
| NDC Code | 50114-6045-2 |
| Proprietary Name | Cocculus compositum |
| Package Description | 100 TABLET in 1 BOTTLE (50114-6045-2) |
| Product NDC | 50114-6045 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ANAMIRTA COCCULUS SEED and CONIUM MACULATUM FLOWERING TOP and AMBERGRIS |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19840131 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Heel Inc. |
| Substance Name | AMBERGRIS; ANAMIRTA COCCULUS SEED; CONIUM MACULATUM FLOWERING TOP |
| Strength Number | 6; 4; 3 |
| Strength Unit | [hp_X]/1; [hp_X]/1; [hp_X]/1 |
| Pharmaceutical Classes |
