Atropine sulfate 0.005 MG/ML / diphenoxylate hydrochloride 0.5 MG/ML Oral Solution — RxCUI 1190568
RxNorm drug concept · Semantic clinical drug
RxCUI 1190568
Semantic clinical drug · SCD
● Current RxNorm concept 1 FDA product
1 package NDC
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
RxCUI1190568
Official nameAtropine sulfate 0.005 MG/ML / diphenoxylate hydrochloride 0.5 MG/ML Oral Solution
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asatropine sulfate 0.025 MG / diphenoxylate HCl 2.5 MG per 5 ML Oral Solution; atropine sulfate 0.025 MG / diphenoxylate HCl 2.5 MG in 5 mL Oral Solution
FDA products mapped1
Package NDCs mapped1
RxNorm release07/06/2026
Snapshot dataJul 14, 2026
📖 Skip the Codes — Read It in Plain English.
Our pharmacist-built guide to Atropine Ophthalmic: what it is, how it’s used, side effects, and interactions.
📗 Our plain-language guide HelloPharmacist
- That's completely expected with atropine — it's actually doing its job. The drop temporarily shuts down the muscle that controls your pupil and your eye's ability to focus, and tho...
- Why does my vision stay blurry and my eyes stay sensitive to light for so long after using these drops?
- Good question! When one eye is significantly stronger than the other, the brain tends to ignore the weaker eye. Putting an atropine drop in the stronger eye blurs it on purpose, so...
- My child's doctor prescribed these drops for lazy eye — how does that work?
🕸️ Concept Web — How Atropine sulfate 0.005 MG/ML / diphenoxylate hyd... 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
Atropine sulfate 0.005 MG/ML / diphenoxylate hydrochloride 0.5 MG/ML Oral Solution
RxCUI 1190568 Semantic clinical drug · SCD
Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.
-
Ingredients 5
The active substance itself — no strength, form, or brand attached yet.
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Atropine
1223IN -
Diphenoxylate
3500IN -
Atropine / diphenoxylate
594040MIN -
Atropine sulfate
153971PIN -
Diphenoxylate hydrochloride
82005PIN
-
Atropine
-
Dose forms 9
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
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Atropine / diphenoxylate Oral Solution
371909SCDF -
Atropine sulfate / diphenoxylate hydrochloride Oral Solution
2647348SCDFP -
Atropine / diphenoxylate Oral Liquid Product
1154667SCDG -
Atropine / diphenoxylate Oral Product
1154668SCDG -
Atropine sulfate / diphenoxylate hydrochloride Oral Liquid Product
2661757SCDGP -
Atropine sulfate / diphenoxylate hydrochloride Oral Product
2662971SCDGP -
Oral Solution
316968DF -
Oral Liquid Product
1151137DFG - +1 more in this family
-
Atropine / diphenoxylate Oral Solution
-
Clinical & branded drugs 2
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
-
Atropine sulfate 0.005 MG/ML
1190566SCDC -
Diphenoxylate hydrochloride 0.5 MG/ML
1190567SCDC
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Atropine sulfate 0.005 MG/ML
Showing up to 8 concepts per family — 15 of 16 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
-
Atropine sulfate 0.005 MG/ML
SCDC · 1190566 -
Diphenoxylate hydrochloride 0.5 MG/ML
SCDC · 1190567 -
Atropine / diphenoxylate Oral Solution
SCDF · 371909 -
Atropine sulfate / diphenoxylate hydrochloride Oral Solution
SCDFP · 2647348 -
Atropine / diphenoxylate Oral Liquid Product
SCDG · 1154667 -
Atropine / diphenoxylate Oral Product
SCDG · 1154668 -
Atropine sulfate / diphenoxylate hydrochloride Oral Liquid Product
SCDGP · 2661757 -
Atropine sulfate / diphenoxylate hydrochloride Oral Product
SCDGP · 2662971
📦 FDA Products & Package NDCs
1 product · 1 package NDC
1 package NDC map to RxCUI 1190568 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 |
|---|---|---|---|---|
| 00054-3194-46 | 1 BOTTLE in 1 CARTON (0054-3194-46) / 60 mL in 1 BOTTLE | Diphenoxylate Hydrochloride and Atropine Sulfate | Hikma Pharmaceuticals USA Inc. | 1982-05-03 |
Observed labelers:
Hikma Pharmaceuticals USA Inc. (1)
— 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.