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Metamucil
Metamucil - 37000-024-02 - (Psyllium Husk)
Drug Information of Metamucil
| Product NDC: | 37000-024 |
| Proprietary Name: | Metamucil |
| Non Proprietary Name: | Psyllium Husk |
| Active Ingredient(s): | 3.4 g/5.8g & nbsp; Psyllium Husk |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Metamucil
| Product NDC: | 37000-024 |
| Labeler Name: | The Procter & Gamble Manufacturing Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19941215 |
Package Information of Metamucil
| Package NDC: | 37000-024-02 |
| Package Description: | 425 g in 1 CANISTER (37000-024-02) |
NDC Information of Metamucil
| NDC Code | 37000-024-02 |
| Proprietary Name | Metamucil |
| Package Description | 425 g in 1 CANISTER (37000-024-02) |
| Product NDC | 37000-024 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Psyllium Husk |
| Dosage Form Name | POWDER |
| Route Name | ORAL |
| Start Marketing Date | 19941215 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | The Procter & Gamble Manufacturing Company |
| Substance Name | PSYLLIUM HUSK |
| Strength Number | 3.4 |
| Strength Unit | g/5.8g |
| Pharmaceutical Classes |
