NDC codes

FDA NDC Directory
Product NDC (as listed)68071-5123Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68071-5123Add 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
68071-5123-56807151230515 mL in 1 BOTTLE, DROPPER (68071-5123-5)Marketed from Dec 6, 2019

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)
Sulfacetamide Sodium
Generic name (nonproprietary)
sulfacetamide sodium
Active ingredients
Sulfacetamide sodium — 100 mg/mL
Dosage form
Solution/ drops
Route
Ophthalmic
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 040066
Marketing start
Listing expires
Other FDA classes
Sulfonamides (Chemical structure)
Identifiers
Product ID 68071-5123_1b54998d-88e0-357a-e063-6394a90a5948SPL ID 1b54998d-88e0-357a-e063-6394a90a5948SPL set ID 9910ec80-e37c-6a83-e053-2995a90a8237RxCUI 1006120UNII 4NRT660KJQUPC 0368071512359
Pharmacologic class
Sulfonamide Antibacterial

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

N468071512305 followed by a unit qualifier and the quantity

Package 68071-5123-05. 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 Sulfacetamide Sodium Ophthalmic Solution, USP 10% is indicated for the treatment of conjunctivitis and other superficial ocular infections due to susceptible microorganisms, and as an adjunctive in systemic sulfonamide therapy of trachoma: Escherichia coli, Staphylococcus aureus, Streptococcus pneumoniae, Streptococcus (viridans group), Haemophilus influenzae, Klebsiella species, and Enterobacter species. Topically applied sulfonamides do not provide adequate coverage against Neisseria species, Serratia marcescens and Pseudomonas aeruginosa . A significant percentage of staphylococcal isolates are completely resistant to sulfa drugs.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 040066

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

FDA NDC Directory listings under ANDA 040066
ProductStrengthForm · routeLabelerProduct NDC
Sulfacetamide SodiumSulfacetamide sodium 100 mg/mLSolution/ dropsOphthalmicA-S Medication Solutions50090-0246
Sulfacetamide SodiumSulfacetamide sodium 100 mg/mLSolution/ dropsOphthalmicBausch & Lomb Incorporated24208-670
Sulfacetamide SodiumSulfacetamide sodium 100 mg/mLSolution/ dropsOphthalmicProficient Rx LP71205-689
Sulfacetamide SodiumSulfacetamide sodium 100 mg/mLSolution/ dropsOphthalmicAsclemed USA, Inc.76420-090
Sulfacetamide SodiumSulfacetamide sodium 100 mg/mLSolution/ dropsOphthalmicPreferred Pharmaceuticals, Inc68788-9871

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