What is NDC 70700-272?

70700-272 is the product NDC for Ramelteon, Ramelteon 8 mg/1 tablet, film coated, listed with the FDA by Xiromed, LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.

Xiromed, LLC, NDC labeler code 70700. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Ramelteon NDC 70700-272 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70700-272Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70700-0272Add 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 NDC	11-digit (billing)	Package
70700-272-05	7070002720570700027205	500 TABLET, FILM COATED in 1 BOTTLE (70700-272-05)Marketed from Nov 25, 2022
70700-272-10	7070002721070700027210	100 TABLET, FILM COATED in 1 BOTTLE (70700-272-10)Marketed from Nov 25, 2022
70700-272-30	7070002723070700027230	30 TABLET, FILM COATED in 1 BOTTLE (70700-272-30)Marketed from Nov 25, 2022

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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: Xiromed, LLCNDC labeler code 70700
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 216209
Marketing start: Nov 25, 2022
Listing expires: Dec 31, 2027
Other FDA classes: Melatonin Receptor Agonists (Mechanism)
Identifiers: Product ID 70700-272_7e963a73-ad79-f5be-3815-e8e6bb74cc30SPL ID 7e963a73-ad79-f5be-3815-e8e6bb74cc30
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

N470700027205 followed by a unit qualifier and the quantity

Package 70700-0272-05. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 70700-272

What is NDC 70700-272?: 70700-272 is the product NDC for Ramelteon, Ramelteon 8 mg/1 tablet, film coated, listed with the FDA by Xiromed, LLC. It has 3 package NDCs, 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?: Xiromed, LLC, NDC labeler code 70700. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Ramelteon	Ramelteon 8 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0593	80425-0593-01
Ramelteon	Ramelteon 8 mg/1	Tablet, Film coatedOral	Marlex Pharmaceuticals, Inc.	10135-838	10135-0838-0110135-0838-30
Ramelteon	Ramelteon 8 mg/1	TabletOral	AvPAK	50268-822	50268-0822-15
Ramelteon	Ramelteon 8 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	72162-2644	72162-2644-0172162-2644-03
Ramelteon	Ramelteon 8 mg/1	Tablet, Film coatedOral	Kanchan Healthcare Inc	85742-023	85742-0023-2285742-0023-23
Ramelteon	Ramelteon 8 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4257	70518-4257-00
Ramelteon	Ramelteon 8 mg/1	TabletOral	Major Pharmaceuticals	0904-7494	00904-7494-06
Ramelteon	Ramelteon 8 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	59651-505	59651-0505-0159651-0505-30
Ramelteon	Ramelteon 8 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-2411	71335-2411-0171335-2411-02
Ramelteon	Ramelteon 8 mg/1	Tablet, Film coatedOral	Asclemed USA, Inc.	76420-880	76420-0880-0176420-0880-3076420-0880-60+1 more

All 38 Ramelteon NDCs

Other NDCs under ANDA 216209

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

FDA NDC Directory listings under ANDA 216209
Product	Strength	Form · route	Labeler	Product NDC
Ramelteon	Ramelteon 8 mg/1	Tablet, Film coatedOral	Golden State Medical Supply, Inc.	51407-523