NDC codes

FDA NDC Directory
Product NDC (as listed)71930-027Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71930-0027Add 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
71930-027-4371930002743473 mL in 1 BOTTLE (71930-027-43)Marketed from Apr 8, 2019

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)
Hydrocodone Bitartrate and Acetaminophen
Generic name (nonproprietary)
hydrocodone bitartrate and acetaminophen
Active ingredients
Hydrocodone bitartrate7.5 mg/15mLAcetaminophen325 mg/15mL
Dosage form
Solution
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 211023
Marketing start
Listing expires
DEA schedule
CII
Other FDA classes
Opioid Agonists (Mechanism)
Identifiers
Product ID 71930-027_f9403954-62f0-42f7-8adb-1de1f26d4aa0SPL ID f9403954-62f0-42f7-8adb-1de1f26d4aa0SPL set ID adb37532-aa19-48a2-95a1-8c92a6ce8651RxCUI 856940UNII NO70W886KK, 362O9ITL9D
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

N471930002743 followed by a unit qualifier and the quantity

Package 71930-0027-43. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 211023

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

FDA NDC Directory listings under ANDA 211023
ProductStrengthForm · routeLabelerProduct NDC
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 7.5 mg/15mL; Acetaminophen 325 mg/15mLSolutionOralRedpharm Drug67296-2166
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 7.5 mg/15mL; Acetaminophen 325 mg/15mLSolutionOralAmerican Health Packaging60687-417

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