What is NDC 27854-701?

27854-701 is the product NDC for Ana-Dent PAIN RELIEF (naproxen sodium), Naproxen sodium 220 mg/1 tablet, film coated, listed with the FDA by Belmora LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Ana-Dent PAIN RELIEF (Naproxen Sodium).

Belmora LLC, NDC labeler code 27854. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Ana-Dent PAIN RELIEF?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Ana-Dent PAIN RELIEF NDC 27854-701

NDC codes

FDA NDC Directory

Product NDC (as listed)27854-701Labeler and product segments. Claims need a package NDC.

Product NDC at billing width27854-0701Add 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	Copy
27854-701-01	2785407010127854070101	1 BOTTLE in 1 CARTON (27854-701-01) / 24 TABLET, FILM COATED in 1 BOTTLEMarketed from May 15, 2020

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): Ana-Dent PAIN RELIEF
Generic name (nonproprietary): naproxen sodium
Active ingredients: Naproxen sodium — 220 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Belmora LLCNDC labeler code 27854
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 205497
Marketing start: May 15, 2020
Listing expires: Dec 31, 2027
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 27854-701_5ac02446-13da-43d5-9647-fe469294acecSPL ID 5ac02446-13da-43d5-9647-fe469294acecSPL set ID 04721306-2850-4e0a-9dd9-7cabb575f3c7RxCUI 849574UNII 9TN87S3A3C
Pharmacologic class: Nonsteroidal Anti-inflammatory Drug

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

N427854070101 followed by a unit qualifier and the quantity

Package 27854-0701-01. 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 May 18, 2020.

Indications (excerpt from the label)

Uses ■ temporarily relieves minor aches and pain due to: ■ headache ■ muscular aches ■ toothache ■ the common cold ■ backache ■ menstrual cramps ■ minor pain of arthritis ■ temporarily reduces fever

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 27854-701

What is NDC 27854-701?: 27854-701 is the product NDC for Ana-Dent PAIN RELIEF (naproxen sodium), Naproxen sodium 220 mg/1 tablet, film coated, listed with the FDA by Belmora LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Ana-Dent PAIN RELIEF (Naproxen Sodium).
What is the active ingredient?: Naproxen sodium.
Who is the labeler?: Belmora LLC, NDC labeler code 27854. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ana-Dent PAIN RELIEF?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other NDCs under ANDA 205497

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

FDA NDC Directory listings under ANDA 205497
Product	Strength	Form · route	Labeler	Product NDC
Naproxen Sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	WALMART INC.	79903-232
Naproxen Sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	WALMART INC.	79903-231
Amazon Basic Care Naproxen Sodiumnaproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Amazon.com Services LLC	72288-366
Naproxen Sodium HEADACHE PAINnaproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Aurohealth LLC	58602-737
Naproxen Sodium HEADACHE PAINnaproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Aurohealth LLC	58602-735
Naproxen Sodium BACK AND MUSCLE PAINnaproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Aurohealth LLC	58602-736
Naproxen Sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Aurohealth LLC	58602-738
Naproxen Sodium BACK AND MUSCLE PAINnaproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Aurohealth LLC	58602-739
Flanax Pain Reliever/Fever Reducernaproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Belmora LLC	27854-700
Naproxen Sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Aurohealth LLC	58602-819
Naproxen Sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Aurohealth LLC	58602-845

Ana-Dent PAIN RELIEF (Naproxen sodium) NDC 27854-701