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SENNAGEN
SENNAGEN - 0182-1093-01 - (Sennosides)
Drug Information of SENNAGEN
| Product NDC: | 0182-1093 |
| Proprietary Name: | SENNAGEN |
| Non Proprietary Name: | Sennosides |
| Active Ingredient(s): | 8.6 mg/1 & nbsp; Sennosides |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SENNAGEN
| Product NDC: | 0182-1093 |
| Labeler Name: | Goldline Laboratories, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20000101 |
Package Information of SENNAGEN
| Package NDC: | 0182-1093-01 |
| Package Description: | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (0182-1093-01) |
NDC Information of SENNAGEN
| NDC Code | 0182-1093-01 |
| Proprietary Name | SENNAGEN |
| Package Description | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (0182-1093-01) |
| Product NDC | 0182-1093 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sennosides |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20000101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Goldline Laboratories, Inc. |
| Substance Name | SENNOSIDES A AND B |
| Strength Number | 8.6 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
