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KENZAPUR
KENZAPUR - 66096-688-17 - (Glonoinum, Lachesis mutus, Natrum muriaticum, Natrum sulphuricum, Thuja occidentalis)
Drug Information of KENZAPUR
| Product NDC: | 66096-688 |
| Proprietary Name: | KENZAPUR |
| Non Proprietary Name: | Glonoinum, Lachesis mutus, Natrum muriaticum, Natrum sulphuricum, Thuja occidentalis |
| Active Ingredient(s): | 12; 6; 6; 6; 9 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp; Glonoinum, Lachesis mutus, Natrum muriaticum, Natrum sulphuricum, Thuja occidentalis |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of KENZAPUR
| Product NDC: | 66096-688 |
| Labeler Name: | OHM PHARMA INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20130701 |
Package Information of KENZAPUR
| Package NDC: | 66096-688-17 |
| Package Description: | 2 BOTTLE, DROPPER in 1 CARTON (66096-688-17) > 50 mL in 1 BOTTLE, DROPPER |
NDC Information of KENZAPUR
| NDC Code | 66096-688-17 |
| Proprietary Name | KENZAPUR |
| Package Description | 2 BOTTLE, DROPPER in 1 CARTON (66096-688-17) > 50 mL in 1 BOTTLE, DROPPER |
| Product NDC | 66096-688 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Glonoinum, Lachesis mutus, Natrum muriaticum, Natrum sulphuricum, Thuja occidentalis |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20130701 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | OHM PHARMA INC. |
| Substance Name | LACHESIS MUTA VENOM; NITROGLYCERIN; SODIUM CHLORIDE; SODIUM SULFATE; THUJA OCCIDENTALIS LEAFY TWIG |
| Strength Number | 12; 6; 6; 6; 9 |
| Strength Unit | [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
| Pharmaceutical Classes |
