Major Heartburn Relief Maximum Strength is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Major Pharmaceuticals. The primary component is Famotidine.
Product ID | 0904-5780_0e4e6213-8767-4f50-900c-ef27d159ca0a |
NDC | 0904-5780 |
Product Type | Human Otc Drug |
Proprietary Name | Major Heartburn Relief Maximum Strength |
Generic Name | Famotidine |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2006-09-29 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA077351 |
Labeler Name | Major Pharmaceuticals |
Substance Name | FAMOTIDINE |
Active Ingredient Strength | 20 mg/1 |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2006-10-04 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA077351 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-09-29 |
Marketing Category | ANDA |
Application Number | ANDA077351 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-10-04 |
Ingredient | Strength |
---|---|
FAMOTIDINE | 20 mg/1 |
SPL SET ID: | ee0a263e-3f78-4534-9a30-803de636f92b |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
0904-5780 | Major Heartburn Relief Maximum Strength | Major Heartburn Relief Maximum Strength |
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 |