NDC codes

FDA NDC Directory
Product NDC (as listed)10702-150Labeler and product segments. Claims need a package NDC.
Product NDC at billing width10702-0150Add 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
10702-150-161070201501610702015016473 mL in 1 BOTTLE (10702-150-16)Marketed from Feb 21, 2017

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 homatropine methylbromide oral solution
Active ingredients
Hydrocodone bitartrate — 5 mg/5mLHomatropine methylbromide — 1.5 mg/5mL
Dosage form
Liquid
Route
Oral
Labeler
KVK-Tech, Inc.NDC labeler code 10702
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 207487
Marketing start
Listing expires
DEA schedule
CII
Other FDA classes
Opioid Agonists (Mechanism)
Identifiers
Product ID 10702-150_526d7f1f-bdeb-5e1f-e063-6294a90a6916SPL ID 526d7f1f-bdeb-5e1f-e063-6294a90a6916SPL set ID 9a737416-08e0-4df6-897e-cf9d1b5f0b01RxCUI 992668UNII NO70W886KK, 68JRS2HC1C
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

N410702015016 followed by a unit qualifier and the quantity

Package 10702-0150-16. 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 homatropine methylbromide is indicated for the symptomatic relief of cough in adult patients 18 years of age and older. Limitations of Use: Not indicated for pediatric patients under 18 years of age [see Use in Specific Populations (8.4)] . Contraindicated in pediatric patients less than 6 years of age [see Contraindications (4)] . Because of the risks of addiction, abuse, misuse, overdose, and death, which can occur at any dosage or duration, and persist over the course of therapy [see Warnings and Precautions (5.1)] , reserve hydrocodone bitartrate and homatropine methylbromide for use in adult patients for whom alternative treatment options are ineffective, not …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 10702-150

What is NDC 10702-150?
10702-150 is the product NDC for Hydrocodone Bitartrate and Homatropine Methylbromide, Hydrocodone bitartrate 5 mg/5mL; Homatropine methylbromide 1.5 mg/5mL liquid, listed with the FDA by KVK-Tech, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Hydrocodone Bitartrate and Homatropine Methylbromide (Hydrocodone bitartrate and homatropine methylbromide oral solution).
What is the active ingredient?
Hydrocodone bitartrate, Homatropine methylbromide.
Who is the labeler?
KVK-Tech, Inc., NDC labeler code 10702. 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 Homatropine Methylbromide?
7 other product NDCs are listed under this name. See all Hydrocodone Bitartrate and Homatropine Methylbromide 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 Homatropine Methylbromide NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Hydrocodone Bitartrate and Homatropine MethylbromideHydrocodone bitartrate 5 mg/5mL; Homatropine methylbromide 1.5 mg/5mLSolutionOralPAI Holdings, LLC dba PAI Pharma0121-103600121-1036-40
Hydrocodone Bitartrate and Homatropine MethylbromideHydrocodone bitartrate 5 mg/1; Homatropine methylbromide 1.5 mg/1TabletOralGenus Lifesciences Inc.64950-20664950-0206-0364950-0206-10
Hydrocodone Bitartrate and Homatropine MethylbromideHydrocodone bitartrate 5 mg/5mL; Homatropine methylbromide 1.5 mg/5mLSolutionOralGenus Lifesciences Inc.64950-37164950-0371-47
Hydrocodone Bitartrate and Homatropine MethylbromideHydrocodone bitartrate 5 mg/1; Homatropine methylbromide 1.5 mg/1TabletOralKVK-Tech, Inc.10702-05510702-0055-0110702-0055-0310702-0055-09+1 more
Hydrocodone Bitartrate and Homatropine MethylbromideHydrocodone bitartrate 5 mg/5mL; Homatropine methylbromide 1.5 mg/5mLSyrupOralNovel Laboratories, Inc.40032-81040032-0810-05
Hydrocodone Bitartrate and Homatropine MethylbromideHydrocodone bitartrate 5 mg/1; Homatropine methylbromide 1.5 mg/1TabletOralNovel Laboratories, Inc.40032-11840032-0118-0340032-0118-2440032-0118-26
Hydrocodone Bitartrate and Homatropine MethylbromideHydrocodone bitartrate 5 mg/1; Homatropine methylbromide 1.5 mg/1TabletOralLupin Pharmaceuticals,Inc.43386-11843386-0118-0143386-0118-03

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