What is NDC 0642-7470?

0642-7470 is the product NDC for Slynd (drospirenone) kit, listed with the FDA by Exeltis USA, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

Exeltis USA, Inc., NDC labeler code 0642. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Slynd?

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.

Slynd NDC 0642-7470 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)0642-7470Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00642-7470Add 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 NDC	11-digit (billing)	Package	Copy
0642-7470-01	0064274700100642747001	1 KIT in 1 CARTON (0642-7470-01) * 24 TABLET, FILM COATED in 1 BLISTER PACK * 4 TABLET, FILM COATED in 1 BLISTER PACKMarketed from Sep 1, 2019
0642-7470-02	0064274700200642747002	1 KIT in 1 CARTON (0642-7470-02) * 24 TABLET, FILM COATED in 1 BLISTER PACK * 4 TABLET, FILM COATED in 1 BLISTER PACKMarketed from Sep 1, 2019 · Sample package

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): Slynd
Generic name (nonproprietary): drospirenone
Dosage form: Kit
Labeler: Exeltis USA, Inc.NDC labeler code 0642
Product type: Prescription drug
Marketing category: NDA — New Drug ApplicationApplication NDA 211367
Marketing start: Jun 6, 2019
Listing expires: Dec 31, 2027
Identifiers: Product ID 0642-7470_5a0ab043-729d-904e-e063-6394a90a0caeSPL ID 5a0ab043-729d-904e-e063-6394a90a0caeSPL set ID db32bc55-f295-4d87-9dbb-0a2f45573dcfRxCUI 748797, 2171000, 2171001, 2171002

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N400642747001 followed by a unit qualifier and the quantity

Package 00642-7470-01. 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 Aug 27, 2026.

Indications (excerpt from the label)

SLYND is a progestin indicated for use by females of reproductive potential to prevent pregnancy. SLYND is a progestin indicated for use by females of reproductive potential to prevent pregnancy. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0642-7470

What is NDC 0642-7470?: 0642-7470 is the product NDC for Slynd (drospirenone) kit, listed with the FDA by Exeltis USA, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Slynd (Drospirenone).
Who is the labeler?: Exeltis USA, Inc., NDC labeler code 0642. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Slynd?: 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.

Slynd (Drospirenone) NDC 0642-7470