NDC codes

FDA NDC Directory
Product NDC (as listed)68071-3555Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68071-3555Add 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
68071-3555-36807135550330 TABLET in 1 BOTTLE (68071-3555-3)Marketed from Dec 21, 2023
68071-3555-66807135550660 TABLET in 1 BOTTLE (68071-3555-6)Marketed from Dec 21, 2023

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
Dicyclomine Hydrochloride
Generic name (nonproprietary)
dicyclomine hydrochloride
Active ingredients
Dicyclomine hydrochloride — 20 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 040317
Marketing start
Listing expires
Other FDA classes
Cholinergic Antagonists (Mechanism)
Identifiers
Product ID 68071-3555_10abba06-dda8-24b2-e063-6394a90a7ae1SPL ID 10abba06-dda8-24b2-e063-6394a90a7ae1SPL set ID 0d07a460-5cb1-cd4b-e063-6294a90a291dRxCUI 991086UNII CQ903KQA31UPC 0368071355536
Pharmacologic class
Anticholinergic

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

N468071355503 followed by a unit qualifier and the quantity

Package 68071-3555-03. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 040317

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

FDA NDC Directory listings under ANDA 040317
ProductStrengthForm · routeLabelerProduct NDC
Dicyclomine HydrochlorideDicyclomine hydrochloride 20 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-665
Dicyclomine HydrochlorideDicyclomine hydrochloride 20 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3606
Dicyclomine HydrochlorideDicyclomine hydrochloride 20 mg/1TabletOralUnit Dose Solutions, Inc.87441-007
Dicyclomine HydrochlorideDicyclomine hydrochloride 20 mg/1TabletOralBryant Ranch Prepack72162-2612
Dicyclomine HydrochlorideDicyclomine hydrochloride 20 mg/1TabletOralRedpharm Drug67296-2154
Dicyclomine HydrochlorideDicyclomine hydrochloride 20 mg/1TabletOralREMEDYREPACK INC.70518-4393
Dicyclomine HydrochlorideDicyclomine hydrochloride 20 mg/1TabletOralCoupler LLC67046-1164
Dicyclomine HydrochlorideDicyclomine hydrochloride 20 mg/1TabletOralAurobindo Pharma Limited59651-720
Dicyclomine HydrochlorideDicyclomine hydrochloride 20 mg/1TabletOralBryant Ranch Prepack71335-2341

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