NDC codes

FDA NDC Directory
Product NDC (as listed)66267-319Labeler and product segments. Claims need a package NDC.
Product NDC at billing width66267-0319Add 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
66267-319-30662670319306626703193030 TABLET in 1 BOTTLE (66267-319-30)Marketed from Jun 11, 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

Generic name (nonproprietary)
hydrocodone bitartrate and acetaminophen
Active ingredients
Hydrocodone bitartrate — 10 mg/1Acetaminophen — 325 mg/1
Dosage form
Tablet
Route
Oral
Labeler
NuCare Pharmaceuticals,Inc.NDC labeler code 66267
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 201013
Marketing start
Listing expires
DEA schedule
CII
Other FDA classes
Opioid Agonists (Mechanism)
Identifiers
Product ID 66267-319_1fa6a518-e720-2232-e063-6294a90a73e4SPL ID 1fa6a518-e720-2232-e063-6294a90a73e4SPL set ID 8b132cf3-c138-59ae-e053-2995a90a98a2RxCUI 856999UNII NO70W886KK, 362O9ITL9DUPC 0366267319300
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

N466267031930 followed by a unit qualifier and the quantity

Package 66267-0319-30. 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)

INDICATIONS AND USAGE Hydrocodone bitartrate and acetaminophen tablets are 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, even at recommended doses [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

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 66267-319

What is NDC 66267-319?
66267-319 is the product NDC for Hydrocodone Bitartrate and Acetaminophen, Hydrocodone bitartrate 10 mg/1; Acetaminophen 325 mg/1 tablet, listed with the FDA by NuCare Pharmaceuticals,Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Hydrocodone Bitartrate and Acetaminophen.
What is the active ingredient?
Hydrocodone bitartrate, Acetaminophen.
Who is the labeler?
NuCare Pharmaceuticals,Inc., NDC labeler code 66267. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Hydrocodone Bitartrate and Acetaminophen?
202 other product NDCs are listed under this name. See all Hydrocodone Bitartrate and Acetaminophen 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 Hydrocodone Bitartrate and Acetaminophen NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 5 mg/1; Acetaminophen 325 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-87360760-0873-3060760-0873-60
Hydrocodone Bitartrate and AcetaminophenAcetaminophen 325 mg/1; Hydrocodone bitartrate 10 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-87260760-0872-3060760-0872-60
hydrocodone bitartrate and acetaminophenHydrocodone bitartrate 5 mg/1; Acetaminophen 325 mg/1TabletOralStrides Pharma Science Limited64380-44064380-0440-01
hydrocodone bitartrate and acetaminophenHydrocodone bitartrate 7.5 mg/1; Acetaminophen 325 mg/1TabletOralStrides Pharma Science Limited64380-44164380-0441-01
hydrocodone bitartrate and acetaminophenHydrocodone bitartrate 10 mg/1; Acetaminophen 325 mg/1TabletOralStrides Pharma Science Limited64380-44264380-0442-01
hydrocodone bitartrate and acetaminophenHydrocodone bitartrate 5 mg/1; Acetaminophen 325 mg/1TabletOralProficient Rx LP82804-30682804-0306-12
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 2.5 mg/1; Acetaminophen 325 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-94031722-0940-01
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 7.5 mg/1; Acetaminophen 325 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-94231722-0942-0131722-0942-05
Hydrocodone Bitartrate And AcetaminophenHydrocodone bitartrate 5 mg/1; Acetaminophen 325 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-87060760-0870-3060760-0870-60
Hydrocodone Bitartrate And AcetaminophenHydrocodone bitartrate 10 mg/15mL; Acetaminophen 300 mg/15mLLiquidOralHikma Pharmaceuticals USA Inc.0054-084300054-0843-63

All 203 Hydrocodone Bitartrate and Acetaminophen NDCs

Other NDCs under ANDA 201013

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

FDA NDC Directory listings under ANDA 201013
ProductStrengthForm · routeLabelerProduct NDC
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 5 mg/1; Acetaminophen 325 mg/1TabletOralAurolife Pharma, LLC13107-019
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 7.5 mg/1; Acetaminophen 325 mg/1TabletOralAurolife Pharma, LLC13107-020
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 10 mg/1; Acetaminophen 325 mg/1TabletOralAurolife Pharma, LLC13107-021
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 5 mg/1; Acetaminophen 325 mg/1TabletOralProficient Rx LP63187-375
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 7.5 mg/1; Acetaminophen 325 mg/1TabletOralProficient Rx LP63187-658
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 10 mg/1; Acetaminophen 325 mg/1TabletOralProficient Rx LP63187-778
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 5 mg/1; Acetaminophen 325 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-4801
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 5 mg/1; Acetaminophen 325 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-4853
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 10 mg/1; Acetaminophen 325 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-4941
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 7.5 mg/1; Acetaminophen 325 mg/1TabletOralBryant Ranch Prepack71335-0108
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 10 mg/1; Acetaminophen 325 mg/1TabletOralBryant Ranch Prepack71335-1271
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 10 mg/1; Acetaminophen 325 mg/1TabletOralBryant Ranch Prepack71335-1339

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