NDC 67618-106
Peri-Colace
Docusate Sodium - Sennosides
Peri-Colace is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Purdue Products Lp. The primary component is Docusate Sodium; Sennosides.
| Product ID | 67618-106_f63ecf22-fb2b-8677-5bfe-c6ac368977a3 |
| NDC | 67618-106 |
| Product Type | Human Otc Drug |
| Proprietary Name | Peri-Colace |
| Generic Name | Docusate Sodium - Sennosides |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 1957-02-08 |
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
| Application Number | part334 |
| Labeler Name | Purdue Products LP |
| Substance Name | DOCUSATE SODIUM; SENNOSIDES |
| Active Ingredient Strength | 50 mg/1; mg/1 |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
Packaging
NDC 67618-106-30
1 BOTTLE, PLASTIC in 1 CARTON (67618-106-30) > 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
| Marketing Start Date | 1957-02-08 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 67618-106-04 [67618010604]
Peri-Colace TABLET, FILM COATED
| Marketing Category | OTC monograph not final |
| Application Number | part334 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 1957-02-08 |
| Inactivation Date | 2019-11-27 |
NDC 67618-106-10 [67618010610]
Peri-Colace TABLET, FILM COATED
| Marketing Category | OTC monograph not final |
| Application Number | part334 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1957-02-08 |
| Inactivation Date | 2019-11-27 |
NDC 67618-106-30 [67618010630]
Peri-Colace TABLET, FILM COATED
| Marketing Category | OTC monograph not final |
| Application Number | part334 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1957-02-08 |
| Inactivation Date | 2019-11-27 |
NDC 67618-106-60 [67618010660]
Peri-Colace TABLET, FILM COATED
| Marketing Category | OTC monograph not final |
| Application Number | part334 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1957-02-08 |
| Inactivation Date | 2019-11-27 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| DOCUSATE SODIUM | 50 mg/1 |
OpenFDA Data
| SPL SET ID: | f63ecf22-fb2b-8677-5bfe-c6ac368977a3 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
Medicade Reported Pricing
67618010660 PERI-COLACE TABLET
Pricing Unit: EA | Drug Type:
67618010630 PERI-COLACE TABLET
Pricing Unit: EA | Drug Type:
67618010610 PERI-COLACE TABLET
Pricing Unit: EA | Drug Type:
NDC Crossover Matching brand name "Peri-Colace" or generic name "Docusate Sodium - Sennosides"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 67618-106 | Peri-Colace | Docusate sodium - sennosides |
| 67618-110 | Colace | Docusate sodium - sennosides |
| 67618-121 | Colace | Docusate sodium - sennosides |
| 70000-0229 | DOCUSATE SODIUM - SENNOSIDES | DOCUSATE SODIUM - SENNOSIDES |
Trademark Results [Peri-Colace]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PERI-COLACE 72024058 0654710 Live/Registered |
MEAD JOHNSON & COMPANY 1957-02-08 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.