NDC codes

FDA NDC Directory
Product NDC (as listed)70518-4768Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-4768Add 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
70518-4768-07051847680070518476800100 POUCH in 1 BOX (70518-4768-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4768-1)Marketed from Oct 8, 2026

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)
Trospium Chloride
Generic name (nonproprietary)
trospium chloride
Active ingredients
Trospium chloride — 20 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
REMEDYREPACK INC.NDC labeler code 70518
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 091575
Marketing start
Listing expires
Other FDA classes
Cholinergic Muscarinic Antagonists (Mechanism)
Identifiers
Product ID 70518-4768_5d54a88e-becb-92f5-e063-6394a90abc3aSPL ID 5d54a88e-becb-92f5-e063-6394a90abc3a
Pharmacologic class
Cholinergic Muscarinic Antagonist

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

N470518476800 followed by a unit qualifier and the quantity

Package 70518-4768-00. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 70518-4768

What is NDC 70518-4768?
70518-4768 is the product NDC for Trospium Chloride, Trospium chloride 20 mg/1 tablet, film coated, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Trospium Chloride.
What is the active ingredient?
Trospium chloride.
Who is the labeler?
REMEDYREPACK INC., NDC labeler code 70518. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Trospium Chloride?
23 other product NDCs are listed under this name. See all Trospium Chloride 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 Trospium Chloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Trospium ChlorideTrospium chloride 20 mg/1Tablet, Film coatedOralMAJOR PHARMACEUTICALS0904-761900904-7619-4000904-7619-52
Trospium ChlorideTrospium chloride 20 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-459370518-4593-0070518-4593-0270518-4593-03+1 more
Trospium ChlorideTrospium chloride 20 mg/1TabletOralMacleods Pharmaceuticals Limited33342-55433342-0554-0933342-0554-39
Trospium ChlorideTrospium chloride 20 mg/1Tablet, Film coatedOralZameer Pharmaceuticals LLC90096-14190096-0141-60
Trospium ChlorideTrospium chloride 60 mg/1Capsule, Extended releaseOralSlate Run Pharmaceuticals, LLC70436-17470436-0174-04
Trospium ChlorideTrospium chloride 60 mg/1Capsule, Extended releaseOralGranules Pharmaceuticals Inc.70010-02770010-0027-0370010-0027-05
Trospium ChlorideTrospium chloride 60 mg/1Capsule, Extended releaseOralProficient Rx LP71205-91771205-0917-0071205-0917-3071205-0917-55+3 more
Trospium ChlorideTrospium chloride 60 mg/1Capsule, Extended releaseOralBluepoint Laboratories68001-42768001-0427-04
Trospium ChlorideTrospium chloride 20 mg/1Tablet, Film coatedOralExelan Pharmaceuticals Inc.76282-33676282-0336-60
Trospium ChlorideTrospium chloride 20 mg/1Tablet, Film coatedOralCIPLA USA INC.,69097-91269097-0912-0269097-0912-0369097-0912-15

All 24 Trospium Chloride NDCs

Other NDCs under ANDA 091575

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

FDA NDC Directory listings under ANDA 091575
ProductStrengthForm · routeLabelerProduct NDC
Trospium ChlorideTrospium chloride 20 mg/1Tablet, Film coatedOralGlenmark Pharmaceuticals Inc., USA68462-461

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