NDC codes

FDA NDC Directory
Product NDC (as listed)71335-9709Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-9709Add 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
71335-9709-17133597090130 CAPSULE in 1 BOTTLE (71335-9709-1)Marketed from May 19, 2023
71335-9709-27133597090290 CAPSULE in 1 BOTTLE (71335-9709-2)Marketed from Dec 28, 2023
71335-9709-37133597090340 CAPSULE in 1 BOTTLE (71335-9709-3)Marketed from Aug 12, 2024
71335-9709-47133597090460 CAPSULE in 1 BOTTLE (71335-9709-4)Marketed from May 18, 2023
71335-9709-57133597090520 CAPSULE in 1 BOTTLE (71335-9709-5)Marketed from Aug 30, 2023
71335-9709-671335970906100 CAPSULE in 1 BOTTLE (71335-9709-6)Marketed from Aug 12, 2024
71335-9709-771335970907180 CAPSULE in 1 BOTTLE (71335-9709-7)Marketed from Aug 12, 2024
71335-9709-871335970908120 CAPSULE in 1 BOTTLE (71335-9709-8)Marketed from Aug 12, 2024
71335-9709-97133597090910 CAPSULE in 1 BOTTLE (71335-9709-9)Marketed from Aug 12, 2024

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 — 10 mg/1
Dosage form
Capsule
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 217054
Marketing start
Listing expires
Other FDA classes
Cholinergic Antagonists (Mechanism)
Identifiers
Product ID 71335-9709_dd3c5206-9f4b-4d4a-b894-7d2046deb58fSPL ID dd3c5206-9f4b-4d4a-b894-7d2046deb58fSPL set ID 4ae8d2fd-a7fb-4cc4-a2cb-720c5a2e2022RxCUI 991061UNII CQ903KQA31
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

N471335970901 followed by a unit qualifier and the quantity

Package 71335-9709-01. 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 .

Indications (excerpt from the label)

Dicyclomine hydrochloride capsules are indicated for the treatment of patients with functional bowel/irritable bowel syndrome. Dicyclomine hydrochloride is an antispasmodic and anticholinergic (antimuscarinic) agent indicated for the treatment of functional bowel/irritable bowel syndrome ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 217054

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

FDA NDC Directory listings under ANDA 217054
ProductStrengthForm · routeLabelerProduct NDC
Dicyclomine HydrochlorideDicyclomine hydrochloride 10 mg/1CapsuleOralUpsher-Smith Laboratories, LLC24979-201
Dicyclomine HydrochlorideDicyclomine hydrochloride 10 mg/1CapsuleOralA-S Medication Solutions50090-7340
Dicyclomine HydrochlorideDicyclomine hydrochloride 10 mg/1CapsuleOralA-S Medication Solutions50090-7341
Dicyclomine HydrochlorideDicyclomine hydrochloride 10 mg/1CapsuleOralAvPAK50268-199
Dicyclomine HydrochlorideDicyclomine hydrochloride 10 mg/1CapsuleOralRedpharm Drug67296-2310
Dicyclomine HydrochlorideDicyclomine hydrochloride 10 mg/1CapsuleOralREMEDYREPACK INC.70518-4432

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