NDC codes

FDA NDC Directory
Product NDC (as listed)85477-712Labeler and product segments. Claims need a package NDC.
Product NDC at billing width85477-0712Add 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 NDC11-digit (billing)PackageCopy
85477-712-30854770712308547707123030 CAPSULE in 1 BOTTLE (85477-712-30)Marketed from Feb 23, 2026

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)
Probentra
Generic name (nonproprietary)
probiotic dietary supplement capsules
Dosage form
Capsule
Route
Oral
Labeler
Oncora Pharma, LLCNDC labeler code 85477
Product type
Prescription drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
Identifiers
Product ID 85477-712_e357f4a7-006b-4dcf-8f8c-8157f5f817efSPL ID e357f4a7-006b-4dcf-8f8c-8157f5f817efSPL set ID 7c0e1b3e-f1a3-451d-a5c6-45bdf13274f8UNII D4S8K64J5Z, K1YRS2QLN2, QFC21096ON, GXW9U52VV9, HTV58LVI9P, N2UDM48ZD6

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

N485477071230 followed by a unit qualifier and the quantity

Package 85477-0712-30. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE Probentra™ is indicated as a probiotic dietary supplement to support digestive health and promote balance of normal intestinal microflora. It is dispensed by prescription and intended for use under medical supervision as part of a dietary supplementation plan. (Notice: no disease treatment claims — this keeps you clean in Rx dietary supplement lane.)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 85477-712

What is NDC 85477-712?
85477-712 is the product NDC for Probentra (probiotic dietary supplement capsules), Lactobacillus acidophilus la 14 400 mg/1 + 5 more ingredients capsule, listed with the FDA by Oncora Pharma, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Probentra (Probiotic Dietary Supplement Capsules).
What is the active ingredient?
Lactobacillus acidophilus la 14, Bifidobacterium animalis lactis bl04, Lactiplantibacillus plantarum, Lacticaseibacillus paracasei lpc-37, Lessonia nigrescens, Beta vulgaris root fructooligosaccharides.
Who is the labeler?
Oncora Pharma, LLC, NDC labeler code 85477. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Probentra?
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.

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