NDC codes

FDA NDC Directory
Product NDC (as listed)60687-700Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60687-0700Add 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
60687-700-0160687070001100 BLISTER PACK in 1 CARTON (60687-700-01) / 1 TABLET in 1 BLISTER PACK (60687-700-11)Marketed from Dec 15, 2022

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

Brand name (proprietary)
Bethanechol Chloride
Generic name (nonproprietary)
bethanechol chloride
Active ingredients
Bethanechol chloride — 25 mg/1
Dosage form
Tablet
Route
Oral
Labeler
American Health PackagingNDC labeler code 60687
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 040855
Marketing start
Listing expires
Other FDA classes
Cholinergic Muscarinic Agonists (Mechanism)
Identifiers
Product ID 60687-700_284e319a-5266-f783-e063-6394a90a7a51SPL ID 284e319a-5266-f783-e063-6394a90a7a51SPL set ID da12a817-9f34-4f26-a7dc-e0e8f9be91c3RxCUI 857321, 857328UNII H4QBZ2LO84
Pharmacologic class
Cholinergic Muscarinic 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

N460687070001 followed by a unit qualifier and the quantity

Package 60687-0700-01. 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)

INDICATIONS AND USAGE Bethanechol chloride tablets are indicated for the treatment of acute postoperative and postpartum nonobstructive (functional) urinary retention and for neurogenic atony of the urinary bladder with retention.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 60687-700

What is NDC 60687-700?
60687-700 is the product NDC for Bethanechol Chloride, Bethanechol chloride 25 mg/1 tablet, listed with the FDA by American Health Packaging. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Bethanechol Chloride.
What is the active ingredient?
Bethanechol chloride.
Who is the labeler?
American Health Packaging, NDC labeler code 60687. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Bethanechol Chloride?
21 other product NDCs are listed under this name. See all Bethanechol 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 Bethanechol Chloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Bethanechol ChlorideBethanechol chloride 10 mg/1TabletOralHeritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc.23155-93523155-0935-01
Bethanechol ChlorideBethanechol chloride 5 mg/1TabletOralHeritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc.23155-93423155-0934-01
Bethanechol ChlorideBethanechol chloride 25 mg/1TabletOralHeritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc.23155-93623155-0936-01
Bethanechol ChlorideBethanechol chloride 50 mg/1TabletOralHeritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc.23155-93723155-0937-01
Bethanechol ChlorideBethanechol chloride 10 mg/1TabletOralAmerican Health Packaging60687-68960687-0689-01
Bethanechol ChlorideBethanechol chloride 5 mg/1TabletOralAmneal Pharmaceuticals of New York LLC53746-57153746-0571-01
Bethanechol ChlorideBethanechol chloride 10 mg/1TabletOralAmneal Pharmaceuticals of New York LLC53746-57253746-0572-01
Bethanechol ChlorideBethanechol chloride 25 mg/1TabletOralAmneal Pharmaceuticals of New York LLC53746-57353746-0573-01
Bethanechol ChlorideBethanechol chloride 50 mg/1TabletOralAmneal Pharmaceuticals of New York LLC53746-57453746-0574-01
Bethanechol ChlorideBethanechol chloride 5 mg/1TabletOralUpsher-Smith Laboratories, LLC0832-051000832-0510-0000832-0510-0100832-0510-10

All 22 Bethanechol Chloride NDCs

Other NDCs under ANDA 040855

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

FDA NDC Directory listings under ANDA 040855
ProductStrengthForm · routeLabelerProduct NDC
Bethanechol ChlorideBethanechol chloride 5 mg/1TabletOralAmneal Pharmaceuticals of New York LLC53746-571
Bethanechol ChlorideBethanechol chloride 10 mg/1TabletOralAmneal Pharmaceuticals of New York LLC53746-572
Bethanechol ChlorideBethanechol chloride 25 mg/1TabletOralAmneal Pharmaceuticals of New York LLC53746-573
Bethanechol ChlorideBethanechol chloride 50 mg/1TabletOralAmneal Pharmaceuticals of New York LLC53746-574
Bethanechol ChlorideBethanechol chloride 50 mg/1TabletOralAmneal Pharmaceuticals LLC65162-574
Bethanechol ChlorideBethanechol chloride 5 mg/1TabletOralAmneal Pharmaceuticals LLC65162-571
Bethanechol ChlorideBethanechol chloride 10 mg/1TabletOralAmneal Pharmaceuticals LLC65162-572
Bethanechol ChlorideBethanechol chloride 25 mg/1TabletOralAmneal Pharmaceuticals LLC65162-573
Bethanechol ChlorideBethanechol chloride 10 mg/1TabletOralAmerican Health Packaging60687-689

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