NDC codes

FDA NDC Directory
Product NDC (as listed)11980-174Labeler and product segments. Claims need a package NDC.
Product NDC at billing width11980-0174Add 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
11980-174-05119800174051 BOTTLE, DROPPER in 1 CARTON (11980-174-05) / 5 mL in 1 BOTTLE, DROPPERMarketed from Dec 1, 1972
11980-174-10119800174101 BOTTLE, DROPPER in 1 CARTON (11980-174-10) / 10 mL in 1 BOTTLE, DROPPERMarketed from Dec 1, 1972

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)
Pred Mild
Generic name (nonproprietary)
prednisolone acetate
Active ingredients
Prednisolone acetate — 1.2 mg/mL
Dosage form
Suspension/ drops
Route
Ophthalmic
Labeler
Allergan, Inc.NDC labeler code 11980
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 017100
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 11980-174_02594e74-d6cf-40b5-bfb1-c27be33e0e35SPL ID 02594e74-d6cf-40b5-bfb1-c27be33e0e35SPL set ID 4fcce64a-94ea-4031-ad5a-c4eddc73a910RxCUI 209002, 562379UNII 8B2807733DUPC 0311980174101
Pharmacologic class
Corticosteroid

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. Ophthalmic products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N411980017405 followed by a unit qualifier and the quantity

Package 11980-0174-05. 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 PRED MILD ® is indicated for the treatment of mild to moderate noninfectious allergic and inflammatory disorders of the lid, conjunctiva, cornea, and sclera (including chemical and thermal burns).

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 11980-174

What is NDC 11980-174?
11980-174 is the product NDC for Pred Mild (prednisolone acetate), Prednisolone acetate 1.2 mg/mL suspension/ drops, listed with the FDA by Allergan, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Pred Mild (Prednisolone acetate).
What is the active ingredient?
Prednisolone acetate.
Who is the labeler?
Allergan, Inc., NDC labeler code 11980. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Pred Mild?
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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