NDC codes

FDA NDC Directory
Product NDC (as listed)73352-917Labeler and product segments. Claims need a package NDC.
Product NDC at billing width73352-0917Add 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
73352-917-407335209174040 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (73352-917-40)Marketed from Mar 23, 2026

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)
Cafergot
Generic name (nonproprietary)
ergotamine tartrate and caffeine
Active ingredients
Ergotamine tartrate — 1 mg/1Caffeine — 100 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Trifluent Pharma, LLCNDC labeler code 73352
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 040590
Marketing start
Listing expires
Other FDA classes
Central Nervous System Stimulation (Physiologic effect)Ergotamines (Chemical structure)Xanthines (Chemical structure)
Identifiers
Product ID 73352-917_4db7f801-0dea-0ec8-e063-6294a90a2636SPL ID 4db7f801-0dea-0ec8-e063-6294a90a2636SPL set ID 4db7eece-2eef-bc1b-e063-6394a90a98cbRxCUI 1293504, 1293506UNII MRU5XH3B48, 3G6A5W338EUPC 0373352917402
Pharmacologic class
Central Nervous System Stimulant; Ergotamine Derivative; Methylxanthine

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

N473352091740 followed by a unit qualifier and the quantity

Package 73352-0917-40. 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 AND USAGE Ergotamine tartrate and caffeine tablets are indicated as therapy to abort or prevent vascular headache; e.g., migraine, migraine variants or so-called “histaminic cephalalgia.”

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 73352-917

What is NDC 73352-917?
73352-917 is the product NDC for Cafergot, Ergotamine tartrate 1 mg/1; Caffeine 100 mg/1 tablet, film coated, listed with the FDA by Trifluent Pharma, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Cafergot (Ergotamine tartrate and caffeine).
What is the active ingredient?
Ergotamine tartrate, Caffeine.
Who is the labeler?
Trifluent Pharma, LLC, NDC labeler code 73352. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Cafergot?
None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other NDCs under ANDA 040590

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

FDA NDC Directory listings under ANDA 040590
ProductStrengthForm · routeLabelerProduct NDC
ergotamine tartrate and caffeineErgotamine tartrate 1 mg/1; Caffeine 100 mg/1Tablet, Film coatedOralCintex Services, LLC24470-917

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