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Aluminum Hydroxide
Aluminum Hydroxide - 0536-0091-85 - (aluminum hydroxide)
Drug Information of Aluminum Hydroxide
| Product NDC: | 0536-0091 |
| Proprietary Name: | Aluminum Hydroxide |
| Non Proprietary Name: | aluminum hydroxide |
| Active Ingredient(s): | 320 mg/5mL & nbsp; aluminum hydroxide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aluminum Hydroxide
| Product NDC: | 0536-0091 |
| Labeler Name: | Rugby Laboratories, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part331 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20050201 |
Package Information of Aluminum Hydroxide
| Package NDC: | 0536-0091-85 |
| Package Description: | 473 mL in 1 BOTTLE (0536-0091-85) |
NDC Information of Aluminum Hydroxide
| NDC Code | 0536-0091-85 |
| Proprietary Name | Aluminum Hydroxide |
| Package Description | 473 mL in 1 BOTTLE (0536-0091-85) |
| Product NDC | 0536-0091 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | aluminum hydroxide |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20050201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rugby Laboratories, Inc. |
| Substance Name | ALUMINUM HYDROXIDE |
| Strength Number | 320 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
