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NDC 43063-0958-95 Docusate Sodium With Sennosides 50; 8.6 mg/1; mg/1 Details
Docusate Sodium With Sennosides 50; 8.6 mg/1; mg/1
Docusate Sodium With Sennosides is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by PD-Rx Pharmaceuticals, Inc.. The primary component is DOCUSATE SODIUM; SENNOSIDES.
MedlinePlus Drug Summary
Senna is used on a short-term basis to treat constipation. It also is used to empty the bowels before surgery and certain medical procedures. Senna is in a class of medications called stimulant laxatives. It works by increasing activity of the intestines to cause a bowel movement.
Related Packages: 43063-0958-95Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Senna
Stool softeners are used on a short-term basis to relieve constipation by people who should avoid straining during bowel movements because of heart conditions, hemorrhoids, and other problems. They work by softening stools to make them easier to pass.
Related Packages: 43063-0958-95Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Stool Softeners
Product Information
| NDC | 43063-0958 |
|---|---|
| Product ID | 43063-958_06d13207-c1fe-8cee-e063-6394a90a21a0 |
| Associated GPIs | 46991002770320 |
| GCN Sequence Number | 048044 |
| GCN Sequence Number Description | sennosides/docusate sodium TABLET 8.6MG-50MG ORAL |
| HIC3 | D6S |
| HIC3 Description | LAXATIVES AND CATHARTICS |
| GCN | 13483 |
| HICL Sequence Number | 021772 |
| HICL Sequence Number Description | SENNOSIDES/DOCUSATE SODIUM |
| Brand/Generic | Generic |
| Proprietary Name | Docusate Sodium With Sennosides |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Docusate Sodium 50mg and Sennosides 8.6mg |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 50; 8.6 |
| Active Ingredient Units | mg/1; mg/1 |
| Substance Name | DOCUSATE SODIUM; SENNOSIDES |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH DRUG |
| Application Number | M007 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 43063-0958-95 (43063095895)
| NDC Package Code | 43063-958-95 |
|---|---|
| Billing NDC | 43063095895 |
| Package | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-958-95) |
| Marketing Start Date | 2019-12-17 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |