What is NDC 51672-2115?

51672-2115 is the product NDC for Feverall Childrens (acetaminophen), Acetaminophen 120 mg/1 suppository, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Feverall Childrens (Acetaminophen).

Sun Pharmaceutical Industries, Inc., NDC labeler code 51672. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Feverall Childrens?

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.

Feverall Childrens NDC 51672-2115 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)51672-2115Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51672-2115Add 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
51672-2115-2	51672211502	6 BLISTER PACK in 1 CARTON (51672-2115-2) / 1 SUPPOSITORY in 1 BLISTER PACK (51672-2115-0)Marketed from Dec 12, 2013
51672-2115-4	51672211504	50 BLISTER PACK in 1 CARTON (51672-2115-4) / 1 SUPPOSITORY in 1 BLISTER PACK (51672-2115-0)Marketed from Dec 12, 2013

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): Feverall ChildrensSuffix: Childrens
Generic name (nonproprietary): acetaminophen
Active ingredients: Acetaminophen — 120 mg/1
Dosage form: Suppository
Route: Rectal
Labeler: Sun Pharmaceutical Industries, Inc.NDC labeler code 51672
Product type: Over-the-counter drug
Marketing category: NDA — New Drug ApplicationApplication NDA 018337
Marketing start: Dec 12, 2013
Listing expires: Dec 31, 2027
Identifiers: Product ID 51672-2115_59cc44c6-9464-1e04-e063-6394a90a7466SPL ID 59cc44c6-9464-1e04-e063-6394a90a7466SPL set ID 861e2987-5473-45b0-b2a6-f980a9b0e809RxCUI 198434, 209353UNII 362O9ITL9D

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N451672211502 followed by a unit qualifier and the quantity

Package 51672-2115-02. 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 Aug 24, 2026.

Indications (excerpt from the label)

Uses temporarily reduces fever relieves minor aches, pains, and headache

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 51672-2115

What is NDC 51672-2115?: 51672-2115 is the product NDC for Feverall Childrens (acetaminophen), Acetaminophen 120 mg/1 suppository, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Feverall Childrens (Acetaminophen).
What is the active ingredient?: Acetaminophen.
Who is the labeler?: Sun Pharmaceutical Industries, Inc., NDC labeler code 51672. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Feverall Childrens?: 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 NDA 018337

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

FDA NDC Directory listings under NDA 018337
Product	Strength	Form · route	Labeler	Product NDC
Feverall Infantsacetaminophen	Acetaminophen 80 mg/1	SuppositoryRectal	Sun Pharmaceutical Industries, Inc.	51672-2114
Feverall Jr. Strengthacetaminophen	Acetaminophen 325 mg/1	SuppositoryRectal	Sun Pharmaceutical Industries, Inc.	51672-2116

Feverall Childrens (Acetaminophen) NDC 51672-2115