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Complete - 37808-321-63 - (famotidine, calcium carbonate and magnesium hydroxide)
Drug Information of Complete
| Product NDC: | 37808-321 |
| Proprietary Name: | Complete |
| Non Proprietary Name: | famotidine, calcium carbonate and magnesium hydroxide |
| Active Ingredient(s): | 800; 10; 165 mg/1; mg/1; mg/1 & nbsp; famotidine, calcium carbonate and magnesium hydroxide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, CHEWABLE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Complete
| Product NDC: | 37808-321 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA077355 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080914 |
Package Information of Complete
| Package NDC: | 37808-321-63 |
| Package Description: | 25 TABLET, CHEWABLE in 1 BOTTLE (37808-321-63) |
NDC Information of Complete
| NDC Code | 37808-321-63 |
| Proprietary Name | Complete |
| Package Description | 25 TABLET, CHEWABLE in 1 BOTTLE (37808-321-63) |
| Product NDC | 37808-321 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | famotidine, calcium carbonate and magnesium hydroxide |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20080914 |
| Marketing Category Name | ANDA |
| Labeler Name | H E B |
| Substance Name | CALCIUM CARBONATE; FAMOTIDINE; MAGNESIUM HYDROXIDE |
| Strength Number | 800; 10; 165 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
