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NDC 70756-0052-12 Famotidine 40 mg/1 Details
Famotidine 40 mg/1
Famotidine is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Lifestar Pharma LLC. The primary component is FAMOTIDINE.
Product Information
| NDC | 70756-0052 |
|---|---|
| Product ID | 70756-052_3f0b58d5-9dce-4423-af1b-feff246a1bfa |
| Associated GPIs | |
| GCN Sequence Number | 011678 |
| GCN Sequence Number Description | famotidine TABLET 40 MG ORAL |
| HIC3 | Z2D |
| HIC3 Description | HISTAMINE H2-RECEPTOR INHIBITORS |
| GCN | 46431 |
| HICL Sequence Number | 004521 |
| HICL Sequence Number Description | FAMOTIDINE |
| Brand/Generic | Generic |
| Proprietary Name | Famotidine |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Famotidine |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 40 |
| Active Ingredient Units | mg/1 |
| Substance Name | FAMOTIDINE |
| Labeler Name | Lifestar Pharma LLC |
| Pharmaceutical Class | Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA075302 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 70756-0052-12 (70756005212)
| NDC Package Code | 70756-052-12 |
|---|---|
| Billing NDC | 70756005212 |
| Package | 1000 TABLET in 1 BOTTLE (70756-052-12) |
| Marketing Start Date | 2023-10-19 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |