NDC codes

FDA NDC Directory
Product NDC (as listed)60687-735Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60687-0735Add 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
60687-735-0160687073501100 BLISTER PACK in 1 CARTON (60687-735-01) / 1 TABLET in 1 BLISTER PACK (60687-735-11)Marketed from Apr 1, 2023

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)
Misoprostol
Generic name (nonproprietary)
misoprostol
Active ingredients
Misoprostol — 100 ug/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076095
Marketing start
Listing expires
Other FDA classes
Synthetic (Chemical structure)
Identifiers
Product ID 60687-735_55064d0e-fa5d-2681-e063-6394a90ad8e8SPL ID 55064d0e-fa5d-2681-e063-6394a90ad8e8SPL set ID 9462d969-d3e5-4e7f-b556-bd647ab28c42RxCUI 311727, 317128UNII 0E43V0BB57
Pharmacologic class
Prostaglandin E1 Analog

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

N460687073501 followed by a unit qualifier and the quantity

Package 60687-0735-01. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS & USAGE Misoprostol is indicated for reducing the risk of NSAID (nonsteroidal anti-inflammatory drugs, including aspirin)–induced gastric ulcers in patients at high risk of complications from gastric ulcer, e.g., the elderly and patients with concomitant debilitating disease, as well as patients at high risk of developing gastric ulceration, such as patients with a history of ulcer. Misoprostol has not been shown to reduce the risk of duodenal ulcers in patients taking NSAIDs. Misoprostol should be taken for the duration of NSAID therapy. Misoprostol has been shown to reduce the risk of gastric ulcers in controlled studies of 3 months' duration. It had no effect, compared to plac…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 076095

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

FDA NDC Directory listings under ANDA 076095
ProductStrengthForm · routeLabelerProduct NDC
MisoprostolMisoprostol 200 ug/1TabletOralGenBioPro, Inc.43393-023
MisoprostolMisoprostol 100 ug/1TabletOralANI Pharmaceuticals, Inc.70954-443
MisoprostolMisoprostol 200 ug/1TabletOralANI Pharmaceuticals, Inc.70954-444
MisoprostolMisoprostol 200 ug/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-300
MisoprostolMisoprostol 100 ug/1TabletOralBryant Ranch Prepack71335-2455
MisoprostolMisoprostol 200 ug/1TabletOralProficient Rx LP82804-037
MisoprostolMisoprostol 100 ug/1TabletOralNuCare Pharmaceuticals, Inc.68071-3762
MisoprostolMisoprostol 200 ug/1TabletOralCardinal Health 107, LLC55154-2145
MisoprostolMisoprostol 200 ug/1TabletOralAmerican Health Packaging60687-746

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