Home
>
National Drug Code (NDC)
>
Almacone
Almacone - 21695-840-12 - (Almacone)
Drug Information of Almacone
| Product NDC: | 21695-840 |
| Proprietary Name: | Almacone |
| Non Proprietary Name: | Almacone |
| Active Ingredient(s): | 200; 200 mg/5mL; mg/5mL & nbsp; Almacone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Almacone
| Product NDC: | 21695-840 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part331 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20081111 |
Package Information of Almacone
| Package NDC: | 21695-840-12 |
| Package Description: | 355 mL in 1 BOTTLE (21695-840-12) |
NDC Information of Almacone
| NDC Code | 21695-840-12 |
| Proprietary Name | Almacone |
| Package Description | 355 mL in 1 BOTTLE (21695-840-12) |
| Product NDC | 21695-840 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Almacone |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20081111 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | ALUMINUM HYDROXIDE; MAGNESIUM HYDROXIDE |
| Strength Number | 200; 200 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
