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Cimicifuga-Homaccord
Cimicifuga-Homaccord - 50114-1032-6 - (BLACK COHOSH and STRONTIUM CARBONATE)
Drug Information of Cimicifuga-Homaccord
| Product NDC: | 50114-1032 |
| Proprietary Name: | Cimicifuga-Homaccord |
| Non Proprietary Name: | BLACK COHOSH and STRONTIUM CARBONATE |
| Active Ingredient(s): | 4; 8 [hp_X]/1.1mL; [hp_X]/1.1mL & nbsp; BLACK COHOSH and STRONTIUM CARBONATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cimicifuga-Homaccord
| Product NDC: | 50114-1032 |
| Labeler Name: | Heel Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 19930131 |
Package Information of Cimicifuga-Homaccord
| Package NDC: | 50114-1032-6 |
| Package Description: | 10 VIAL in 1 CARTON (50114-1032-6) > 1.1 mL in 1 VIAL |
NDC Information of Cimicifuga-Homaccord
| NDC Code | 50114-1032-6 |
| Proprietary Name | Cimicifuga-Homaccord |
| Package Description | 10 VIAL in 1 CARTON (50114-1032-6) > 1.1 mL in 1 VIAL |
| Product NDC | 50114-1032 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BLACK COHOSH and STRONTIUM CARBONATE |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 19930131 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Heel Inc |
| Substance Name | BLACK COHOSH; STRONTIUM CARBONATE |
| Strength Number | 4; 8 |
| Strength Unit | [hp_X]/1.1mL; [hp_X]/1.1mL |
| Pharmaceutical Classes |
