Famotidine is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Carlsbad Technology, Inc. The primary component is Famotidine.
| Product ID | 61442-121_88518123-8f7b-4eb7-a1a1-a94c7d422141 |
| NDC | 61442-121 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Famotidine |
| Generic Name | Famotidine |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2001-04-16 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA075805 |
| Labeler Name | Carlsbad Technology, Inc |
| Substance Name | FAMOTIDINE |
| Active Ingredient Strength | 20 mg/1 |
| Pharm Classes | Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 2001-04-16 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA075805 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2001-04-16 |
| Marketing Category | ANDA |
| Application Number | ANDA075805 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2001-04-16 |
| Marketing Category | ANDA |
| Application Number | ANDA075805 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2001-04-16 |
| Marketing Category | ANDA |
| Application Number | ANDA075805 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2001-04-16 |
| Ingredient | Strength |
|---|---|
| FAMOTIDINE | 20 mg/1 |
| SPL SET ID: | a8b5c855-053d-4295-8f57-1a96a6ccaa92 |
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