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NDC 78206-0137-01 FOSAMAX PLUS D 70; 2800 mg/1; [iU]/1 Details
FOSAMAX PLUS D 70; 2800 mg/1; [iU]/1
FOSAMAX PLUS D is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Organon LLC. The primary component is ALENDRONATE SODIUM; CHOLECALCIFEROL.
Product Information
| NDC | 78206-0137 |
|---|---|
| Product ID | 78206-137_587e47f6-6e25-4379-8263-9fc44f72718e |
| Associated GPIs | 30042010200370 |
| GCN Sequence Number | 058947 |
| GCN Sequence Number Description | alendronate sodium/vitamin D3 TABLET 70 MG-2800 ORAL |
| HIC3 | P4N |
| HIC3 Description | BONE RESORPTION INHIBITOR AND VITAMIN D COMBS. |
| GCN | 24481 |
| HICL Sequence Number | 032841 |
| HICL Sequence Number Description | ALENDRONATE SODIUM/CHOLECALCIFEROL (VITAMIN D3) |
| Brand/Generic | Brand |
| Proprietary Name | FOSAMAX PLUS D |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | ALENDRONATE SODIUM and CHOLECALCIFEROL |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 70; 2800 |
| Active Ingredient Units | mg/1; [iU]/1 |
| Substance Name | ALENDRONATE SODIUM; CHOLECALCIFEROL |
| Labeler Name | Organon LLC |
| Pharmaceutical Class | Bisphosphonate [EPC], Diphosphonates [CS], Vitamin D [CS], Vitamin D [EPC] |
| DEA Schedule | n/a |
| Marketing Category | NDA |
| Application Number | NDA021762 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 78206-0137-01 (78206013701)
| NDC Package Code | 78206-137-01 |
|---|---|
| Billing NDC | 78206013701 |
| Package | 4 TABLET in 1 BLISTER PACK (78206-137-01) |
| Marketing Start Date | 2021-06-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |