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ConRx AR
ConRx AR - 68737-237-21 - (ALUMINUM HYDROXIDE and MAGNESIUM HYDROXIDE)
Drug Information of ConRx AR
| Product NDC: | 68737-237 |
| Proprietary Name: | ConRx AR |
| Non Proprietary Name: | ALUMINUM HYDROXIDE and MAGNESIUM HYDROXIDE |
| Active Ingredient(s): | 160; 105 mg/1; mg/1 & nbsp; ALUMINUM HYDROXIDE and MAGNESIUM HYDROXIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, CHEWABLE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ConRx AR
| Product NDC: | 68737-237 |
| Labeler Name: | Eagle Distributors,Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part331 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130318 |
Package Information of ConRx AR
| Package NDC: | 68737-237-21 |
| Package Description: | 50 POUCH in 1 BOX (68737-237-21) > 1 TABLET, CHEWABLE in 1 POUCH |
NDC Information of ConRx AR
| NDC Code | 68737-237-21 |
| Proprietary Name | ConRx AR |
| Package Description | 50 POUCH in 1 BOX (68737-237-21) > 1 TABLET, CHEWABLE in 1 POUCH |
| Product NDC | 68737-237 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALUMINUM HYDROXIDE and MAGNESIUM HYDROXIDE |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20130318 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Eagle Distributors,Inc. |
| Substance Name | ALUMINUM HYDROXIDE; MAGNESIUM HYDROXIDE |
| Strength Number | 160; 105 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
