What is NDC 37808-883?

37808-883 is the product NDC for HEB Anti Nausea, Dextrose, Unspecified form 1.87 g/5mL + 2 more ingredients liquid, listed with the FDA by HEB. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

HEB Anti Nausea (Dextrose(glucose),Levulose(fructose),Phosphoric acid).

What is the active ingredient?

Dextrose, Unspecified form, Fructose, Phosphoric acid.

HEB, NDC labeler code 37808. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for HEB Anti Nausea?

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.

HEB Anti Nausea NDC 37808-883 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)37808-883Labeler and product segments. Claims need a package NDC.

Product NDC at billing width37808-0883Add 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
37808-883-04	37808088304	1 BOTTLE in 1 CARTON (37808-883-04) / 118 mL in 1 BOTTLEMarketed from Apr 20, 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): HEB Anti Nausea
Generic name (nonproprietary): dextrose(glucose),levulose(fructose),phosphoric acid
Active ingredients: Dextrose, Unspecified form — 1.87 g/5mLFructose — 1.87 g/5mLPhosphoric acid — 21.5 mg/5mL
Dosage form: Liquid
Route: Oral
Labeler: HEBNDC labeler code 37808
Product type: Over-the-counter drug
Marketing category: Unapproved drug (other)
Marketing start: Apr 20, 2020
Listing expires: Dec 31, 2027
Identifiers: Product ID 37808-883_63bc4f59-58de-4cc0-ae80-d52ea4832f14SPL ID 63bc4f59-58de-4cc0-ae80-d52ea4832f14

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

N437808088304 followed by a unit qualifier and the quantity

Package 37808-0883-04. 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 37808-883

What is NDC 37808-883?: 37808-883 is the product NDC for HEB Anti Nausea, Dextrose, Unspecified form 1.87 g/5mL + 2 more ingredients liquid, listed with the FDA by HEB. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: HEB Anti Nausea (Dextrose(glucose),Levulose(fructose),Phosphoric acid).
What is the active ingredient?: Dextrose, Unspecified form, Fructose, Phosphoric acid.
Who is the labeler?: HEB, NDC labeler code 37808. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for HEB Anti Nausea?: 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.