NDC codes

FDA NDC Directory
Product NDC (as listed)72189-649Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72189-0649Add 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
72189-649-207218906492020 TABLET in 1 BOTTLE (72189-649-20)Marketed from Nov 25, 2025
72189-649-307218906493030 TABLET in 1 BOTTLE (72189-649-30)Marketed from Nov 25, 2025
72189-649-607218906496060 TABLET in 1 BOTTLE (72189-649-60)Marketed from Nov 25, 2025

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/APAP
Generic name (nonproprietary)
hydrocodone/apap
Active ingredients
Hydrocodone bitartrate — 5 mg/1Acetaminophen — 325 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Direct_Rx
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 210211
Marketing start
Listing expires
DEA schedule
CII
Other FDA classes
Opioid Agonists (Mechanism)
Identifiers
Product ID 72189-649_4a188f02-629f-25cf-e063-6394a90a5766SPL ID 4a188f02-629f-25cf-e063-6394a90a5766SPL set ID 446f01f0-2853-d104-e063-6394a90ae351RxCUI 857002UNII 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

N472189064920 followed by a unit qualifier and the quantity

Package 72189-0649-20. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

Hydrocodone Bitartrate and Acetaminophen Tablet is indicated for the management of pain severe enough to require an opioid analgesic and for which alternative treatments are inadequate. Limitations of Use Because of the risks of addiction, abuse, and misuse, with opioids, which can occur at dosage or duration [see WARNINGS], reserve Hydrocodone Bitartrate and Acetaminophen Tablets for use in patients for whom alternative treatment options [e.g., non-opioid analgesics] have not been tolerated, or are not expected to be tolerated, have not provided adequate analgesia, or are not expected to provide adequate analgesia Hydrocodone Bitartrate and Acetaminophen Tablets should not be used for an ex…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 210211

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

FDA NDC Directory listings under ANDA 210211
ProductStrengthForm · routeLabelerProduct NDC
Hydrocodone/APAPHydrocodone bitartrate 10 mg/1; Acetaminophen 325 mg/1TabletOralDirect_Rx72189-650
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 5 mg/1; Acetaminophen 325 mg/1TabletOralBryant Ranch Prepack71335-2116
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 5 mg/1; Acetaminophen 325 mg/1TabletOralBryant Ranch Prepack63629-8885
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 10 mg/1; Acetaminophen 325 mg/1TabletOralBryant Ranch Prepack63629-8886
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 5 mg/1; Acetaminophen 325 mg/1TabletOralBryant Ranch Prepack71335-2144
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 5 mg/1; Acetaminophen 325 mg/1TabletOralRedpharm Drug67296-2201
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 5 mg/1; Acetaminophen 325 mg/1TabletOralBryant Ranch Prepack72162-1989
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 7.5 mg/1; Acetaminophen 325 mg/1TabletOralBryant Ranch Prepack72162-1990
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 10 mg/1; Acetaminophen 325 mg/1TabletOralBryant Ranch Prepack72162-1991
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 10 mg/1; Acetaminophen 325 mg/1TabletOralAsclemed USA, Inc.87063-051
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 5 mg/1; Acetaminophen 325 mg/1TabletOralAsclemed USA, Inc.87063-049
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 7.5 mg/1; Acetaminophen 325 mg/1TabletOralAsclemed USA, Inc.87063-050
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 5 mg/1; Acetaminophen 325 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3447
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 5 mg/1; Acetaminophen 325 mg/1TabletOralBryant Ranch Prepack63629-1939
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 10 mg/1; Acetaminophen 325 mg/1TabletOralBryant Ranch Prepack63629-1938
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 7.5 mg/1; Acetaminophen 325 mg/1TabletOralBryant Ranch Prepack63629-1940
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 7.5 mg/1; Acetaminophen 325 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-2494
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 7.5 mg/1; Acetaminophen 325 mg/1TabletOralBryant Ranch Prepack71335-1970
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 5 mg/1; Acetaminophen 325 mg/1TabletOralAmerican Health Packaging60687-396
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 7.5 mg/1; Acetaminophen 325 mg/1TabletOralAmerican Health Packaging60687-407

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