NDC codes

FDA NDC Directory
Product NDC (as listed)87063-050Labeler and product segments. Claims need a package NDC.
Product NDC at billing width87063-0050Add 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
87063-050-018706300500187063005001100 TABLET in 1 BOTTLE (87063-050-01)Marketed from Nov 24, 2025
87063-050-0587063005005870630050055 TABLET in 1 BOTTLE (87063-050-05)Marketed from Nov 24, 2025
87063-050-0787063005007870630050077 TABLET in 1 BOTTLE (87063-050-07)Marketed from Nov 24, 2025
87063-050-10870630050108706300501010 TABLET in 1 BOTTLE (87063-050-10)Marketed from Nov 24, 2025
87063-050-14870630050148706300501414 TABLET in 1 BOTTLE (87063-050-14)Marketed from Nov 24, 2025
87063-050-20870630050208706300502020 TABLET in 1 BOTTLE (87063-050-20)Marketed from Nov 24, 2025
87063-050-30870630050308706300503030 TABLET in 1 BOTTLE (87063-050-30)Marketed from Nov 24, 2025
87063-050-60870630050608706300506060 TABLET in 1 BOTTLE (87063-050-60)Marketed from Nov 24, 2025
87063-050-90870630050908706300509090 TABLET in 1 BOTTLE (87063-050-90)Marketed from Nov 24, 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

Generic name (nonproprietary)
hydrocodone bitartrate and acetaminophen
Active ingredients
Hydrocodone bitartrate — 7.5 mg/1Acetaminophen — 325 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Asclemed USA, Inc.NDC labeler code 87063
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 87063-050_4ca4b03b-efbe-4d32-e063-6394a90af0f3SPL ID 4ca4b03b-efbe-4d32-e063-6394a90af0f3SPL set ID 66e184cd-fa32-431f-b843-9c4bea12593bRxCUI 856999, 857002, 857005UNII 362O9ITL9D, NO70W886KK
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

N487063005001 followed by a unit qualifier and the quantity

Package 87063-0050-01. 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

Current FDA label (SPL), effective . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE 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 shoul…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 87063-050

What is NDC 87063-050?
87063-050 is the product NDC for Hydrocodone Bitartrate and Acetaminophen, Hydrocodone bitartrate 7.5 mg/1; Acetaminophen 325 mg/1 tablet, listed with the FDA by Asclemed USA, Inc.. It has 9 package NDCs, 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?
Asclemed USA, Inc., NDC labeler code 87063. 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?
201 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 10 mg/1; Acetaminophen 325 mg/1TabletOralStrides Pharma Science Limited64380-44264380-0442-01
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 5 mg/1; Acetaminophen 325 mg/1TabletOralProficient Rx LP82804-30682804-0306-12
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 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 10 mg/15mL; Acetaminophen 300 mg/15mLLiquidOralHikma Pharmaceuticals USA Inc.0054-084300054-0843-63

All 202 Hydrocodone Bitartrate and Acetaminophen NDCs

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 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
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 10 mg/1; Acetaminophen 325 mg/1TabletOralAmerican Health Packaging60687-418
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 10 mg/1; Acetaminophen 325 mg/1TabletOralBryant Ranch Prepack63629-1938
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 5 mg/1; Acetaminophen 325 mg/1TabletOralBryant Ranch Prepack63629-1939
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 7.5 mg/1; Acetaminophen 325 mg/1TabletOralBryant Ranch Prepack63629-1940
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/1TabletOralRedpharm Drug67296-2201
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/1TabletOralNuCare Pharmaceuticals,Inc.68071-2645
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 5 mg/1; Acetaminophen 325 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3447
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/1TabletOralBryant Ranch Prepack71335-2116
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/1TabletOralEywa Pharma Inc71930-019
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 7.5 mg/1; Acetaminophen 325 mg/1TabletOralEywa Pharma Inc71930-020
Hydrocodone Bitartrate and AcetaminophenHydrocodone bitartrate 10 mg/1; Acetaminophen 325 mg/1TabletOralEywa Pharma Inc71930-021
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

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