up and up famotidine is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Target Corporation. The primary component is Famotidine.
Product ID | 11673-031_0d6f2ac0-295e-47ce-aedb-8cadc1e66a63 |
NDC | 11673-031 |
Product Type | Human Otc Drug |
Proprietary Name | up and up famotidine |
Generic Name | Famotidine |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2015-03-13 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA075400 |
Labeler Name | Target Corporation |
Substance Name | FAMOTIDINE |
Active Ingredient Strength | 10 mg/1 |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2015-03-13 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA075400 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-03-13 |
Ingredient | Strength |
---|---|
FAMOTIDINE | 10 mg/1 |
SPL SET ID: | 0d6f2ac0-295e-47ce-aedb-8cadc1e66a63 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
11673-061 | up and up famotidine | up and up famotidine |
11673-031 | up and up famotidine | up and up famotidine |
0363-0141 | Acid Controller | Famotidine |
0363-0701 | Acid Controller | Famotidine |
0363-1203 | acid controller | famotidine |
0113-7141 | basic care acid reducer | Famotidine |
0113-7194 | Basic Care famotidine | Famotidine |
0093-2748 | Famotidine | Famotidine |
0172-5728 | Famotidine | Famotidine |
0172-5729 | Famotidine | Famotidine |
0338-5197 | Famotidine | Famotidine |
0363-0036 | Famotidine | Famotidine |
0363-1899 | Famotidine | Famotidine |
0113-0141 | good sense acid reducer | Famotidine |
0113-0194 | Good Sense Acid Reducer | Famotidine |
0187-4420 | Pepcid | famotidine |
0187-4440 | Pepcid | famotidine |