What is NDC 54973-6440?

54973-6440 is the product NDC for Nat Sulph (sodium sulfate anhydrous), Sodium sulfate anhydrous 6 [hp_X]/1 tablet, listed with the FDA by Hyland's Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Nat Sulph (Sodium sulfate anhydrous).

Hyland's Inc., NDC labeler code 54973. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Nat Sulph?

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.

Nat Sulph NDC 54973-6440 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)54973-6440Labeler and product segments. Claims need a package NDC.

Product NDC at billing width54973-6440Add 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
54973-6440-1	5497364400154973644001	500 TABLET in 1 BOTTLE, PLASTIC (54973-6440-1)Marketed from Jan 1, 1940
54973-6440-2	5497364400254973644002	1000 TABLET in 1 BOTTLE, PLASTIC (54973-6440-2)Marketed from Jan 1, 1940

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): Nat Sulph
Generic name (nonproprietary): sodium sulfate anhydrous
Active ingredients: Sodium sulfate anhydrous — 6 [hp_X]/1
Dosage form: Tablet
Route: Oral
Labeler: Hyland's Inc.NDC labeler code 54973
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 1, 1940
Listing expires: Dec 31, 2026
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)
Identifiers: Product ID 54973-6440_f03141f6-9def-7d57-e053-2995a90a16aeSPL ID f03141f6-9def-7d57-e053-2995a90a16aeSPL set ID 84d12830-b34f-415d-a19a-947c5040d8bfUNII 36KCS0R750UPC 0354973644014
Pharmacologic class: Osmotic Laxative

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

N454973644001 followed by a unit qualifier and the quantity

Package 54973-6440-01. 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 Dec 19, 2022.

Indications (excerpt from the label)

INDICATIONS Relief of symptoms of the flu,nausea and vomiting.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 54973-6440

What is NDC 54973-6440?: 54973-6440 is the product NDC for Nat Sulph (sodium sulfate anhydrous), Sodium sulfate anhydrous 6 [hp_X]/1 tablet, listed with the FDA by Hyland's Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Nat Sulph (Sodium sulfate anhydrous).
What is the active ingredient?: Sodium sulfate anhydrous.
Who is the labeler?: Hyland's Inc., NDC labeler code 54973. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Nat Sulph?: 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.

Nat Sulph (Sodium sulfate anhydrous) NDC 54973-6440