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Ammonium Lactate
Ammonium Lactate - 63044-404-20 - (Ammonium Lactate)
Drug Information of Ammonium Lactate
| Product NDC: | 63044-404 |
| Proprietary Name: | Ammonium Lactate |
| Non Proprietary Name: | Ammonium Lactate |
| Active Ingredient(s): | 17 g/g & nbsp; Ammonium Lactate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ammonium Lactate
| Product NDC: | 63044-404 |
| Labeler Name: | Nnodum Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20071230 |
Package Information of Ammonium Lactate
| Package NDC: | 63044-404-20 |
| Package Description: | 140 g in 1 TUBE (63044-404-20) |
NDC Information of Ammonium Lactate
| NDC Code | 63044-404-20 |
| Proprietary Name | Ammonium Lactate |
| Package Description | 140 g in 1 TUBE (63044-404-20) |
| Product NDC | 63044-404 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ammonium Lactate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20071230 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Nnodum Pharmaceuticals |
| Substance Name | AMMONIUM LACTATE |
| Strength Number | 17 |
| Strength Unit | g/g |
| Pharmaceutical Classes |
