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Medique Diotame
Medique Diotame - 47682-220-33 - (BISMUTH SUBSALICYLATE)
Drug Information of Medique Diotame
| Product NDC: | 47682-220 |
| Proprietary Name: | Medique Diotame |
| Non Proprietary Name: | BISMUTH SUBSALICYLATE |
| Active Ingredient(s): | 262 mg/1 & nbsp; BISMUTH SUBSALICYLATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, CHEWABLE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Medique Diotame
| Product NDC: | 47682-220 |
| Labeler Name: | Unifirst First Aid Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part335 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20081230 |
Package Information of Medique Diotame
| Package NDC: | 47682-220-33 |
| Package Description: | 50 PACKET in 1 BOX, UNIT-DOSE (47682-220-33) > 2 TABLET, CHEWABLE in 1 PACKET (47682-220-99) |
NDC Information of Medique Diotame
| NDC Code | 47682-220-33 |
| Proprietary Name | Medique Diotame |
| Package Description | 50 PACKET in 1 BOX, UNIT-DOSE (47682-220-33) > 2 TABLET, CHEWABLE in 1 PACKET (47682-220-99) |
| Product NDC | 47682-220 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BISMUTH SUBSALICYLATE |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20081230 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Unifirst First Aid Corporation |
| Substance Name | BISMUTH SUBSALICYLATE |
| Strength Number | 262 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
