Alendronic acid 70 MG / cholecalciferol 2800 UNT Oral Tablet [Fosamax Plus D] — RxCUI 904495
RxNorm drug concept · Semantic branded drug
RxCUI 904495
Semantic branded drug · SBD
● Current RxNorm concept 2 FDA products
2 package NDCs
Snapshot Jul 14, 2026
What you’re looking at: the standardized identity of one medicine, as the U.S. drug-data system sees it. Below — every FDA-listed product, package code, price benchmark, and billing code that maps to it.
🗂️ Key Facts
RxCUI904495
Official nameAlendronic acid 70 MG / cholecalciferol 2800 UNT Oral Tablet [Fosamax Plus D]
Concept typeSemantic branded drug (SBD)
RxNorm statusCurrent RxNorm concept
Also known asFosamax Plus D 70/2800 Oral Tablet; FOSAMAX PLUS D 70 MG / 2800 UNT Oral Tablet; Fosamax Plus D 70/2800 (alendronic acid / vitamin D3) Oral Tablet
FDA products mapped2
Package NDCs mapped2
Reported Medicaid activity (SDUD)631 prescriptions · 3 state & territory Medicaid programs · latest period Q4 2025
RxNorm release07/06/2026
Snapshot dataJul 14, 2026
📖 Skip the Codes — Read It in Plain English.
Our pharmacist-built guide to Alendronate: what it is, how it’s used, side effects, and interactions.
📗 Our plain-language guide HelloPharmacist
- It strengthens bone and lowers fracture risk in osteoporosis. Some products are also used for steroid-induced osteoporosis and Paget's disease of bone. Your pharmacy label shows wh...
- Take it first thing in the morning with a full glass of plain water, at least 30 minutes before food, drinks or other medicines. Stay upright for at least 30 minutes and until you...
- Stomach upset, heartburn, nausea, constipation or diarrhea, and some bone or muscle aches can happen. Stop and call your doctor if you have trouble or pain swallowing, chest pain,...
- What side effects are normal, and when should I call?
🕸️ Concept Web — How Alendronic acid 70 MG / cholecalciferol 2800 UNT... Connects
One RxCUI never lives alone. Follow the path from the raw ingredient down to the exact strength-and-form concepts FDA products carry — every stop is a real RxNorm concept with its own identifier. Hover or focus any chip for what it means.
This page's concept
Alendronic acid 70 MG / cholecalciferol 2800 UNT Oral Tablet [Fosamax Plus D]
RxCUI 904495 Semantic branded drug · SBD
Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.
-
Ingredients 4
The active substance itself — no strength, form, or brand attached yet.
-
Alendronate
46041IN -
Cholecalciferol
2418IN -
Alendronate / cholecalciferol
1007560MIN -
Alendronic acid
236083PIN
-
Alendronate
-
Brand names 1
The same medicine's trade names. A brand name alone says nothing about strength or form.
-
Fosamax Plus D
607553BN
-
Fosamax Plus D
-
Dose forms 13
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
-
Alendronate / cholecalciferol Oral Tablet
904461SCDF -
Alendronic acid / cholecalciferol Oral Tablet
2645980SCDFP -
Alendronate / cholecalciferol Oral Product
1367006SCDG -
Alendronate / cholecalciferol Pill
1367007SCDG -
Alendronic acid / cholecalciferol Oral Product
2661789SCDGP -
Alendronic acid / cholecalciferol Pill
2660037SCDGP -
Alendronate / cholecalciferol Oral Tablet [Fosamax Plus D]
904464SBDF -
Alendronic acid / cholecalciferol Oral Tablet [Fosamax Plus D]
2654887SBDFP - +5 more in this family
-
Alendronate / cholecalciferol Oral Tablet
-
Clinical & branded drugs 4
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
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Alendronic acid 70 MG / cholecalciferol 2800 UNT Oral Tablet
904492SCD -
Alendronic acid 70 MG
904430SCDC -
Cholecalciferol 2800 UNT
584612SCDC -
Alendronic acid 70 MG / cholecalciferol 2800 UNT [Fosamax Plus D]
904493SBDC
-
Alendronic acid 70 MG / cholecalciferol 2800 UNT Oral Tablet
Showing up to 8 concepts per family — 17 of 22 stored related concepts drawn.
These are official RxNorm vocabulary relationships — how concepts name and organize the same medicine. They do not establish therapeutic equivalence or substitutability: two concepts appearing in one web is never a statement that products can be swapped.
🔀 Generic ⇄ Brand Crosswalk
The same medicine has an unbranded (generic) identity and one or more brand-name identities — each with its own RxCUI. This is a naming relationship in RxNorm, not a statement that any two products are substitutable.
Generic (Clinical) Concepts
-
Alendronic acid 70 MG / cholecalciferol 2800 UNT Oral Tablet
SCD · 904492 -
Alendronic acid 70 MG
SCDC · 904430 -
Cholecalciferol 2800 UNT
SCDC · 584612 -
Alendronate / cholecalciferol Oral Tablet
SCDF · 904461 -
Alendronic acid / cholecalciferol Oral Tablet
SCDFP · 2645980 -
Alendronate / cholecalciferol Oral Product
SCDG · 1367006 -
Alendronate / cholecalciferol Pill
SCDG · 1367007 -
Alendronic acid / cholecalciferol Oral Product
SCDGP · 2661789 -
Alendronic acid / cholecalciferol Pill
SCDGP · 2660037
Brand-Name Concepts
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Alendronic acid 70 MG / cholecalciferol 2800 UNT [Fosamax Plus D]
SBDC · 904493 -
Alendronate / cholecalciferol Oral Tablet [Fosamax Plus D]
SBDF · 904464 -
Alendronic acid / cholecalciferol Oral Tablet [Fosamax Plus D]
SBDFP · 2654887 -
Fosamax Plus D Oral Product
SBDG · 1173287 -
Fosamax Plus D Pill
SBDG · 1173288 -
Fosamax Plus D
BN · 607553
📦 FDA Products & Package NDCs
2 products · 2 package NDCs
2 package NDCs map to RxCUI 904495 in the current snapshot — up to 50 per page. Each linked NDC opens its full package page.
| Package NDC | Package | Brand / generic name | Labeler | Marketing start |
|---|---|---|---|---|
| 78206-0136-01 | 4 TABLET in 1 BLISTER PACK (78206-136-01) | FOSAMAX PLUS D | Organon LLC | 2021-06-01 |
| 78206-0137-01 | 4 TABLET in 1 BLISTER PACK (78206-137-01) | FOSAMAX PLUS D | Organon LLC | 2021-06-01 |
Observed labelers:
Organon LLC (2)
— this is the FDA-listed mapping footprint, not sales, inventory, availability, or market share.
🗃️ Sources & Limits
Atlas generation902fddb9-e9c1-4004-bf4c-dba4d51037c7
openFDA export observedJul 14, 2026
RxNorm release07/06/2026
Methodology2026-07-full-catalog-v1
- A shared RxCUI does not prove interchangeability. Products mapped to the same concept are not thereby equivalent or substitutable — equivalence is a separate, product-level determination.
- Listing here does not establish approval or coverage. Appearing in this snapshot is a data observation, not an FDA approval status or a payer coverage decision.
- Missing data never means zero. A silent dataset (no price, no billing code, no utilization) means no observation — not that the real-world value is zero.
- Counts describe the mapping footprint. Product, package, and labeler counts are the FDA-listed mapping footprint in this snapshot — not sales, inventory, availability, or market share.
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product.
Reference information about drug-concept identifiers and public regulatory data — not medical advice. Talk to your pharmacist or prescriber about your own medication.