NDC codes

FDA NDC Directory
Product NDC (as listed)40032-118Labeler and product segments. Claims need a package NDC.
Product NDC at billing width40032-0118Add 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
40032-118-03400320118034003201180330 TABLET in 1 BOTTLE (40032-118-03)Marketed from Sep 23, 2014
40032-118-244003201182440032011824100 TABLET in 1 BOTTLE (40032-118-24)Marketed from Sep 23, 2014
40032-118-264003201182640032011826500 TABLET in 1 BOTTLE (40032-118-26)Marketed from Sep 23, 2014

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
Active ingredients
Hydrocodone bitartrate — 5 mg/1Homatropine methylbromide — 1.5 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Novel Laboratories, Inc.NDC labeler code 40032
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 091528
Marketing start
Listing expires
DEA schedule
CII
Other FDA classes
Opioid Agonists (Mechanism)
Identifiers
Product ID 40032-118_ced58732-29db-4f15-a4d4-858f3e4ecc4eSPL ID ced58732-29db-4f15-a4d4-858f3e4ecc4eSPL set ID b203c87c-1108-4eaa-8a57-87be776d8a70RxCUI 992656UNII NO70W886KK, 68JRS2HC1CUPC 0340032118039, 0340032118244
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

N440032011803 followed by a unit qualifier and the quantity

Package 40032-0118-03. 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 Tablets are 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, and misuse with opioids, even at recommended doses [ see Warnings and Precautions (5.1) ] , reserve Hydrocodone Bitartrate and Homatropine Methylbromide Tablets for use in adult patients for whom the benefits of cough suppression are expected to outweigh the risks, and in whom an adequ…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 40032-118

What is NDC 40032-118?
40032-118 is the product NDC for Hydrocodone Bitartrate and Homatropine Methylbromide, Hydrocodone bitartrate 5 mg/1; Homatropine methylbromide 1.5 mg/1 tablet, listed with the FDA by Novel Laboratories, Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Hydrocodone Bitartrate and Homatropine Methylbromide.
What is the active ingredient?
Hydrocodone bitartrate, Homatropine methylbromide.
Who is the labeler?
Novel Laboratories, Inc., NDC labeler code 40032. 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 and homatropine methylbromide oral solutionHydrocodone bitartrate 5 mg/5mL; Homatropine methylbromide 1.5 mg/5mLLiquidOralKVK-Tech, Inc.10702-15010702-0150-16
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/1TabletOralLupin Pharmaceuticals,Inc.43386-11843386-0118-0143386-0118-03

Other NDCs under ANDA 091528

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

FDA NDC Directory listings under ANDA 091528
ProductStrengthForm · routeLabelerProduct NDC
Hydrocodone Bitartrate and Homatropine MethylbromideHydrocodone bitartrate 5 mg/1; Homatropine methylbromide 1.5 mg/1TabletOralLupin Pharmaceuticals,Inc.43386-118

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