What is NDC 62207-814?

62207-814 is the product NDC for Naproxen Sodium and Diphenhydramine HCl, Naproxen sodium 220 mg/1; Diphenhydramine hydrochloride 25 mg/1 tablet, film coated, listed with the FDA by Granules India Ltd. It has 4 package NDCs, shown above in 10- and 11-digit form.

What is the active ingredient?

Naproxen sodium, Diphenhydramine hydrochloride.

Granules India Ltd, NDC labeler code 62207. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Naproxen Sodium and Diphenhydramine HCl?

2 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Naproxen Sodium and Diphenhydramine HCl NDC 62207-814

NDC codes

FDA NDC Directory

Product NDC (as listed)62207-814Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62207-0814Add 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
62207-814-38	6220708143862207081438	37500 TABLET, FILM COATED in 1 POUCH (62207-814-38)Marketed from Feb 20, 2021
62207-814-39	6220708143962207081439	7500 TABLET, FILM COATED in 1 POUCH (62207-814-39)Marketed from Feb 20, 2021
62207-814-47	6220708144762207081447	500 TABLET, FILM COATED in 1 BOTTLE (62207-814-47)Marketed from Feb 20, 2021
62207-814-95	6220708149562207081495	1 BOTTLE in 1 CARTON (62207-814-95) / 20 TABLET, FILM COATED in 1 BOTTLEMarketed from Feb 20, 2021

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): Naproxen Sodium and Diphenhydramine HCl
Generic name (nonproprietary): naproxen sodium and diphenhydramine hcl
Active ingredients: Naproxen sodium — 220 mg/1Diphenhydramine hydrochloride — 25 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Granules India LtdNDC labeler code 62207
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 213663
Marketing start: Feb 20, 2021
Listing expires: Dec 31, 2027
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 62207-814_5d3efc04-4a22-8ac6-e063-6394a90a1a76SPL ID 5d3efc04-4a22-8ac6-e063-6394a90a1a76
Pharmacologic class: Histamine-1 Receptor Antagonist; 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

N462207081438 followed by a unit qualifier and the quantity

Package 62207-0814-38. 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 62207-814

What is NDC 62207-814?: 62207-814 is the product NDC for Naproxen Sodium and Diphenhydramine HCl, Naproxen sodium 220 mg/1; Diphenhydramine hydrochloride 25 mg/1 tablet, film coated, listed with the FDA by Granules India Ltd. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Naproxen Sodium and Diphenhydramine HCl.
What is the active ingredient?: Naproxen sodium, Diphenhydramine hydrochloride.
Who is the labeler?: Granules India Ltd, NDC labeler code 62207. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Naproxen Sodium and Diphenhydramine HCl?: 2 other product NDCs are listed under this name. See all Naproxen Sodium and Diphenhydramine HCl 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 Naproxen Sodium and Diphenhydramine HCl NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Naproxen Sodium and Diphenhydramine HCL	Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1	TabletOral	TARGET CORPORATION	11673-819	11673-0819-08
Naproxen Sodium and Diphenhydramine HClnaproxen sodium and diphenhydramine	Naproxen sodium 220 mg/1; Diphenhydramine hydrochloride 25 mg/1	Tablet, Film coatedOral	Amneal Pharmaceuticals NY LLC	69238-1422	69238-1422-0269238-1422-0469238-1422-06+1 more

Other NDCs under ANDA 213663

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

FDA NDC Directory listings under ANDA 213663
Product	Strength	Form · route	Labeler	Product NDC
Naproxen Sodium and Diphenhydramine HCL	Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1	TabletOral	TARGET CORPORATION	11673-819
Naproxen Sodium Diphenhydramine HCl	Naproxen sodium 220 mg/1; Diphenhydramine hydrochloride 25 mg/1	Tablet, Film coatedOral	CVS PHARMACY, INC	69842-328
Naproxen Sodium Diphenhydramine HCL	Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1	TabletOral	Walmart	79903-204
Naproxen Sodium Diphenhydramine Hydrochloride	Naproxen sodium 220 mg/1; Diphenhydramine hydrochloride 25 mg/1	TabletOral	SAFEWAY	21130-814