NDC codes

FDA NDC Directory
Product NDC (as listed)70199-017Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70199-0017Add 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
70199-017-017019900170170199001701100 TABLET in 1 BOTTLE (70199-017-01)Marketed from Nov 27, 2019
70199-017-30701990017307019900173030 TABLET in 1 BOTTLE (70199-017-30)Marketed from Nov 27, 2019

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)
Thalitone
Generic name (nonproprietary)
chlorthalidone
Active ingredients
Chlorthalidone — 15 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Casper Pharma LLCNDC labeler code 70199
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 019574
Marketing start
Listing expires
Other FDA classes
Increased Diuresis (Physiologic effect)
Identifiers
Product ID 70199-017_fd617814-535d-4aa0-a182-cadbc691781dSPL ID fd617814-535d-4aa0-a182-cadbc691781dSPL set ID bc5a0299-115b-4e60-bb3f-c75a95c51c15RxCUI 197498, 197499, 214081, 214083UNII Q0MQD1073Q
Pharmacologic class
Thiazide-like Diuretic

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

N470199001701 followed by a unit qualifier and the quantity

Package 70199-0017-01. 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)

THALITONE is a thiazide-like diuretic indicated: • For the treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions (1.1). • as adjunctive therapy in edema associated with heart failure, cirrhosis of the liver, and renal disease, including nephrotic syndrome (1.2). 1.1 Hypertension THALITONE ® is indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. These benefits have been seen in controlled trials of antihypertensive dru…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70199-017

What is NDC 70199-017?
70199-017 is the product NDC for Thalitone (chlorthalidone), Chlorthalidone 15 mg/1 tablet, listed with the FDA by Casper Pharma LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Thalitone (Chlorthalidone).
What is the active ingredient?
Chlorthalidone.
Who is the labeler?
Casper Pharma LLC, NDC labeler code 70199. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Thalitone?
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.

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