Pepcid Complete is a Oral Tablet, Chewable in the Human Otc Drug category. It is labeled and distributed by Johnson & Johnson Consumer Inc., Mcneil Consumer Healthcare Division. The primary component is Famotidine; Calcium Carbonate; Magnesium Hydroxide.
Product ID | 16837-246_7e17cbcf-29c7-41cc-924a-149ed90bb258 |
NDC | 16837-246 |
Product Type | Human Otc Drug |
Proprietary Name | Pepcid Complete |
Generic Name | Famotidine, Calcium Carbonate, And Magnesium Hydroxide |
Dosage Form | Tablet, Chewable |
Route of Administration | ORAL |
Marketing Start Date | 2009-01-01 |
Marketing Category | NDA / NDA |
Application Number | NDA020958 |
Labeler Name | Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division |
Substance Name | FAMOTIDINE; CALCIUM CARBONATE; MAGNESIUM HYDROXIDE |
Active Ingredient Strength | 10 mg/1; mg/1; mg/1 |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2009-01-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA020958 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-01-01 |
Marketing Category | NDA |
Application Number | NDA020958 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-01-01 |
Marketing End Date | 2013-03-31 |
Marketing Category | NDA |
Application Number | NDA020958 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-01-01 |
Marketing End Date | 2014-03-31 |
Marketing Category | NDA |
Application Number | NDA020958 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-01-01 |
Marketing End Date | 2014-03-24 |
Marketing Category | NDA |
Application Number | NDA020958 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-01-01 |
Marketing End Date | 2013-03-31 |
Marketing Category | NDA |
Application Number | NDA020958 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-01-01 |
Marketing End Date | 2013-05-31 |
Marketing Category | NDA |
Application Number | NDA020958 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-01-01 |
Marketing End Date | 2012-03-31 |
Marketing Category | NDA |
Application Number | NDA020958 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-01-01 |
Marketing End Date | 2016-04-11 |
Marketing Category | NDA |
Application Number | NDA020958 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-01-01 |
Marketing End Date | 2014-01-24 |
Marketing Category | NDA |
Application Number | NDA020958 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-01-01 |
Ingredient | Strength |
---|---|
FAMOTIDINE | 10 mg/1 |
SPL SET ID: | 37e6a3f6-5261-475d-a7d4-e72854088982 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
16837-246 | Pepcid Complete | Famotidine, Calcium Carbonate, and Magnesium Hydroxide |
16837-298 | Pepcid Complete | Famotidine, Calcium carbonate, and Magnesium hydroxide |
16837-891 | Pepcid Complete | famotidine, calcium carbonate, and magnesium hydroxide |
50269-016 | Pepcid Complete | FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE |
52904-948 | Pepcid Complete | Famotidine, Calcium Carbonate, and Magnesium Hydroxide |
66715-9822 | Pepcid Complete | Famotidine, Calcium Carbonate, Magnesium Hydroxide Chewable Tablet |
67751-202 | Pepcid Complete | Famotidine, Calcium carbonate, and Magnesium hydroxide |
70264-034 | Pepcid Complete | famotidine, calcium carbonate, and magnesium hydroxide |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PEPCID COMPLETE 86459772 4772806 Live/Registered |
JOHNSON & JOHNSON 2014-11-20 |
PEPCID COMPLETE 76165191 2629164 Dead/Cancelled |
JOHNSON & JOHNSON 2000-11-15 |