NDC codes

FDA NDC Directory
Product NDC (as listed)60758-119Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60758-0119Add 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
60758-119-05607580119051 BOTTLE, DROPPER in 1 CARTON (60758-119-05) / 5 mL in 1 BOTTLE, DROPPERMarketed from Aug 19, 1997
60758-119-10607580119101 BOTTLE, DROPPER in 1 CARTON (60758-119-10) / 10 mL in 1 BOTTLE, DROPPERMarketed from Aug 19, 1997
60758-119-15607580119151 BOTTLE, DROPPER in 1 CARTON (60758-119-15) / 15 mL in 1 BOTTLE, DROPPERMarketed from Aug 19, 1997

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)
Prednisolone Acetate
Generic name (nonproprietary)
prednisolone acetate
Active ingredients
Prednisolone acetate — 10 mg/mL
Dosage form
Suspension/ drops
Route
Ophthalmic
Labeler
Pacific Pharma, Inc.NDC labeler code 60758
Product type
Prescription drug
Marketing category
NDA authorized genericApplication NDA 017011
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 60758-119_9bb24539-c1ac-4ce6-88a8-a5dfad588c27SPL ID 9bb24539-c1ac-4ce6-88a8-a5dfad588c27SPL set ID 1474d1df-70b6-4b1e-86d1-3349aa6d42fbRxCUI 1376336UNII 8B2807733DUPC 0360758119103
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

N460758011905 followed by a unit qualifier and the quantity

Package 60758-0119-05. 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 Prednisolone acetate ophthalmic suspension 1% is indicated for the treatment of steroid-responsive inflammation of the palpebral and bulbar conjunctiva, cornea, and anterior segment of the globe.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 60758-119

What is NDC 60758-119?
60758-119 is the product NDC for Prednisolone Acetate, Prednisolone acetate 10 mg/mL suspension/ drops, listed with the FDA by Pacific Pharma, Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Prednisolone Acetate.
What is the active ingredient?
Prednisolone acetate.
Who is the labeler?
Pacific Pharma, Inc., NDC labeler code 60758. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Prednisolone Acetate?
14 other product NDCs are listed under this name. See all Prednisolone Acetate NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Prednisolone Acetate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
prednisolone acetatePrednisolone acetate 10 mg/mLSuspension/ dropsOphthalmicAmneal Pharmaceuticals NY LLC60219-255060219-2550-01
prednisolone acetatePrednisolone acetate 10 mg/mLSuspension/ dropsOphthalmicAmneal Pharmaceuticals NY LLC60219-255160219-2551-01
prednisolone acetatePrednisolone acetate 10 mg/mLSuspension/ dropsOphthalmicAmneal Pharmaceuticals NY LLC60219-255260219-2552-01
Prednisolone AcetatePrednisolone acetate 10 mg/mLSuspension/ dropsOphthalmicLupin Pharmaceuticals, Inc.70748-33270748-0332-0270748-0332-0370748-0332-04
Prednisolone AcetatePrednisolone acetate 10 mg/mLSuspension/ dropsOphthalmicRedpharm Drug67296-217667296-2176-05
Prednisolone AcetatePrednisolone acetate 10 mg/mLSuspension/ dropsOphthalmicA-S Medication Solutions50090-753950090-7539-00
Prednisolone AcetatePrednisolone acetate 10 mg/mLSuspension/ dropsOphthalmicA-S Medication Solutions50090-527550090-5275-00
Prednisolone AcetatePrednisolone acetate 10 mg/mLSuspension/ dropsOphthalmicNuCare Pharmaceuticals,Inc.68071-222268071-2222-05
Prednisolone AcetatePrednisolone acetate 10 mg/mLSuspension/ dropsOphthalmicA-S Medication Solutions50090-191250090-1912-00
Prednisolone AcetatePrednisolone acetate 10 mg/mLSuspension/ dropsOphthalmicSportpharm LLC85766-12485766-0124-05

All 15 Prednisolone Acetate NDCs

Other NDCs under NDA 017011

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

FDA NDC Directory listings under NDA 017011
ProductStrengthForm · routeLabelerProduct NDC
Prednisolone AcetatePrednisolone acetate 10 mg/mLSuspension/ dropsOphthalmicA-S Medication Solutions50090-5275
Prednisolone AcetatePrednisolone acetate 10 mg/mLSuspension/ dropsOphthalmicNuCare Pharmaceuticals,Inc.68071-2222
Prednisolone AcetatePrednisolone acetate 10 mg/mLSuspension/ dropsOphthalmicA-S Medication Solutions50090-1912
Prednisolone AcetatePrednisolone acetate 10 mg/mLSuspension/ dropsOphthalmicSportpharm LLC85766-124
Prednisolone AcetatePrednisolone acetate 10 mg/mLSuspension/ dropsOphthalmicAsclemed USA, Inc.76420-204
Pred Forteprednisolone acetatePrednisolone acetate 10 mg/mLSuspension/ dropsOphthalmicAllergan, Inc.11980-180

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