NDC codes

FDA NDC Directory
Product NDC (as listed)0527-1699Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00527-1699Add 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
0527-1699-0100527169901100 TABLET in 1 BOTTLE (0527-1699-01)Marketed from Jun 13, 2014

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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)
Codeine Sulfate
Generic name (nonproprietary)
codeine sulfate
Active ingredients
Codeine sulfate — 60 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 203046
Marketing start
Listing expires
DEA schedule
CII
Other FDA classes
Full Opioid Agonists (Mechanism)
Identifiers
Product ID 0527-1699_aa8c1550-c22e-4945-8664-7a3d66523843SPL ID aa8c1550-c22e-4945-8664-7a3d66523843SPL set ID 5819bdf7-300e-45b8-8f3a-447b53656293RxCUI 997170, 997287, 997296UNII 11QV9BS0CBUPC 0305271699015
Pharmacologic class
Opioid Agonist

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

N400527169901 followed by a unit qualifier and the quantity

Package 00527-1699-01. 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

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