NDC codes

FDA NDC Directory
Product NDC (as listed)80425-0203Labeler and product segments. Claims need a package NDC.
Product NDC at billing width80425-0203Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
80425-0203-1804250203018042502030130 TABLET, FILM COATED in 1 BOTTLE (80425-0203-1)Marketed from Jun 30, 2020

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Ramelteon
Generic name (nonproprietary)
ramelteon
Active ingredients
Ramelteon — 8 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Advanced Rx Pharmacy of Tennessee, LLCNDC labeler code 80425
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 212650
Marketing start
Listing expires
Other FDA classes
Melatonin Receptor Agonists (Mechanism)
Identifiers
Product ID 80425-0203_2a99c981-daf6-71e5-e063-6294a90a5c1dSPL ID 2a99c981-daf6-71e5-e063-6294a90a5c1dSPL set ID ed37ac7c-ab7e-57b3-e053-2995a90a5b90RxCUI 577348UNII 901AS54I69
Pharmacologic class
Melatonin Receptor Agonist

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N480425020301 followed by a unit qualifier and the quantity

Package 80425-0203-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

1. Indications and Usage Ramelteon Tablets are indicated for the treatment of insomnia characterized by difficulty with sleep onset. The clinical trials performed in support of efficacy were up to six months in duration. The final formal assessments of sleep latency were performed after two days of treatment during the crossover study (elderly only), at five weeks in the six week studies (adults and elderly), and at the end of the six month study (adults and elderly) [see CLINICAL STUDIES (14)].

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 80425-0203

What is NDC 80425-0203?
80425-0203 is the product NDC for Ramelteon, Ramelteon 8 mg/1 tablet, film coated, listed with the FDA by Advanced Rx Pharmacy of Tennessee, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Ramelteon.
What is the active ingredient?
Ramelteon.
Who is the labeler?
Advanced Rx Pharmacy of Tennessee, LLC, NDC labeler code 80425. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ramelteon?
37 other product NDCs are listed under this name. See all Ramelteon NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Ramelteon NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
RamelteonRamelteon 8 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-059380425-0593-01
RamelteonRamelteon 8 mg/1Tablet, Film coatedOralMarlex Pharmaceuticals, Inc.10135-83810135-0838-0110135-0838-30
RamelteonRamelteon 8 mg/1TabletOralAvPAK50268-82250268-0822-15
RamelteonRamelteon 8 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-264472162-2644-0172162-2644-03
RamelteonRamelteon 8 mg/1Tablet, Film coatedOralKanchan Healthcare Inc85742-02385742-0023-2285742-0023-23
RamelteonRamelteon 8 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-425770518-4257-00
RamelteonRamelteon 8 mg/1TabletOralMajor Pharmaceuticals0904-749400904-7494-06
RamelteonRamelteon 8 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-50559651-0505-0159651-0505-30
RamelteonRamelteon 8 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-241171335-2411-0171335-2411-02
RamelteonRamelteon 8 mg/1Tablet, Film coatedOralAsclemed USA, Inc.76420-88076420-0880-0176420-0880-3076420-0880-60+1 more

All 38 Ramelteon NDCs

Other NDCs under ANDA 212650

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 212650
ProductStrengthForm · routeLabelerProduct NDC
RamelteonRamelteon 8 mg/1Tablet, Film coatedOralTruPharma, LLC52817-235
RamelteonRamelteon 8 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-2186
RamelteonRamelteon 8 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-2886
RamelteonRamelteon 8 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-2176
RamelteonRamelteon 8 mg/1Tablet, Film coatedOralDirect_Rx72189-369
RamelteonRamelteon 8 mg/1Tablet, Film coatedOrali3 Pharmaceuticals, LLC72319-005
RamelteonRamelteon 8 mg/1Tablet, Film coatedOralProficient Rx LP82804-216

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