United States· US:43598-741_54220029-c5df-b277-af7e-2786da03bbed
Ramelteon
A ramelteon product containing ramelteon, registered in United States by Dr.Reddys Laboratories Inc.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- RAMELTEON
- Manufacturer
- Dr.Reddys Laboratories Inc
- Country
- United States (US)
- ATC code
- N05CH02
- ATC class
- Ramelteon
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- July 26, 2026
Packs & prices · 4
- ndc1143598-741-30
- ndc114359874101100 TABLET in 1 BOTTLE (43598-741-01)
- ndc11435987413030 TABLET in 1 BOTTLE (43598-741-30)
- ndc1143598-741-01
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
132 interactions on record for ramelteon.
Graded by severity as the source publishes them — 4 severe. Severity grades are free for everyone; mechanism and management come with Growth.
- Severity for every pair — free, no plan needed
- The source, licence and sync date on every record
- Mechanism and what to do for each pair — Growth plan
Ramelteon · interactions on record
132 records
- 4 severe
- 128 moderate
Most severe, free to view
- MorphineN02AA01severe
- MorphinN07BC09severe
- HydrocodoneR05DA03severe
- CodeineR05DA04severe
- Interaction severity from DDInter 2.0 (Xiong G. et al., Nucleic Acids Res.), licensed CC BY-NC 4.0 — free for non-commercial use only; not covered by the Drug Database commercial licence.
Same class
Other records under N05CH02
Ramelteon, as other registers publish it.
- United StatesRamelteonSportpharm LLC
- United StatesRamelteonBryant Ranch Prepack
- United StatesRamelteonAvPAK
- United StatesRamelteonUpsher-Smith Laboratories, LLC
- United StatesRamelteonMajor Pharmaceuticals
- United StatesRamelteonBryant Ranch Prepack
- United StatesRamelteonMicro Labs Limited
- United StatesRamelteonActavis Pharma, Inc.
Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.
For developers
The same record over the API, and the raw payload
GET /v1/drugs/3ee16208-e82a-4b2f-9271-6fea93fad975 GET /v1/drugs/3ee16208-e82a-4b2f-9271-6fea93fad975?format=fhir
Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.
{
"route": "ORAL",
"source": "ndc",
"strength": "8",
"substance": "RAMELTEON",
"productndc": "43598-741",
"dosage_form": "TABLET",
"dea_schedule": null,
"strength_unit": "mg/1",
"application_number": "ANDA091693",
"marketing_category": "ANDA"
}See everything about ramelteon.
This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.