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AMMONIUM LACTATE
AMMONIUM LACTATE - 0574-2121-28 - (AMMONIUM LACTATE)
Drug Information of AMMONIUM LACTATE
| Product NDC: | 0574-2121 |
| 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: | 0574-2121 |
| Labeler Name: | Paddock Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076829 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060207 |
Package Information of AMMONIUM LACTATE
| Package NDC: | 0574-2121-28 |
| Package Description: | 2 TUBE in 1 CARTON (0574-2121-28) > 140 g in 1 TUBE |
NDC Information of AMMONIUM LACTATE
| NDC Code | 0574-2121-28 |
| Proprietary Name | AMMONIUM LACTATE |
| Package Description | 2 TUBE in 1 CARTON (0574-2121-28) > 140 g in 1 TUBE |
| Product NDC | 0574-2121 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | AMMONIUM LACTATE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20060207 |
| Marketing Category Name | ANDA |
| Labeler Name | Paddock Laboratories, Inc. |
| Substance Name | AMMONIUM LACTATE |
| Strength Number | 120 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
