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NDC 00115-1681-26 Alendronate Sodium 70 mg/1 Details
Alendronate Sodium 70 mg/1
Alendronate Sodium is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals of New York LLC. The primary component is ALENDRONATE SODIUM.
Product Information
| NDC | 00115-1681 |
|---|---|
| Product ID | 0115-1681_0bb7b70c-72e0-4bb8-9d3a-0fc8e4762dd1 |
| Associated GPIs | 30042010100370 |
| GCN Sequence Number | 046941 |
| GCN Sequence Number Description | alendronate sodium TABLET 70 MG ORAL |
| HIC3 | P4L |
| HIC3 Description | BONE RESORPTION INHIBITORS |
| GCN | 85361 |
| HICL Sequence Number | 010124 |
| HICL Sequence Number Description | ALENDRONATE SODIUM |
| Brand/Generic | Generic |
| Proprietary Name | Alendronate Sodium |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Alendronate Sodium |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 70 |
| Active Ingredient Units | mg/1 |
| Substance Name | ALENDRONATE SODIUM |
| Labeler Name | Amneal Pharmaceuticals of New York LLC |
| Pharmaceutical Class | Bisphosphonate [EPC], Diphosphonates [CS] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA075710 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 00115-1681-26 (00115168126)
| NDC Package Code | 0115-1681-26 |
|---|---|
| Billing NDC | 00115168126 |
| Package | 12 BLISTER PACK in 1 CARTON (0115-1681-26) / 1 TABLET in 1 BLISTER PACK (0115-1681-30) |
| Marketing Start Date | 2008-02-06 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |