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Lac Hydrin
Lac Hydrin - 10631-099-28 - (ammonium lactate)
Drug Information of Lac Hydrin
| Product NDC: | 10631-099 |
| Proprietary Name: | Lac Hydrin |
| 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 Lac Hydrin
| Product NDC: | 10631-099 |
| Labeler Name: | Ranbaxy Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020508 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090316 |
Package Information of Lac Hydrin
| Package NDC: | 10631-099-28 |
| Package Description: | 140 g in 1 TUBE (10631-099-28) |
NDC Information of Lac Hydrin
| NDC Code | 10631-099-28 |
| Proprietary Name | Lac Hydrin |
| Package Description | 140 g in 1 TUBE (10631-099-28) |
| Product NDC | 10631-099 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ammonium lactate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20090316 |
| Marketing Category Name | NDA |
| Labeler Name | Ranbaxy Laboratories Inc. |
| Substance Name | AMMONIUM LACTATE |
| Strength Number | 120 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
