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Ammonium Lactate
Ammonium Lactate - 51672-1301-0 - (Ammonium Lactate)
Drug Information of Ammonium Lactate
| Product NDC: | 51672-1301 |
| Proprietary Name: | Ammonium Lactate |
| Non Proprietary Name: | Ammonium Lactate |
| Active Ingredient(s): | 120 mg/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: | 51672-1301 |
| Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075883 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030410 |
Package Information of Ammonium Lactate
| Package NDC: | 51672-1301-0 |
| Package Description: | 385 g in 1 BOTTLE, PLASTIC (51672-1301-0) |
NDC Information of Ammonium Lactate
| NDC Code | 51672-1301-0 |
| Proprietary Name | Ammonium Lactate |
| Package Description | 385 g in 1 BOTTLE, PLASTIC (51672-1301-0) |
| Product NDC | 51672-1301 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ammonium Lactate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20030410 |
| Marketing Category Name | ANDA |
| Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
| Substance Name | AMMONIUM LACTATE |
| Strength Number | 120 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
