What is NDC 50742-359?

50742-359 is the product NDC for Progesterone, Progesterone 100 mg/1 insert, listed with the FDA by Ingenus Pharmaceuticals, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Ingenus Pharmaceuticals, LLC, NDC labeler code 50742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Progesterone?

77 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Progesterone NDC 50742-359 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)50742-359Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50742-0359Add 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
50742-359-21	5074203592150742035921	1 CARTON in 1 CARTON (50742-359-21) / 21 BLISTER PACK in 1 CARTON (50742-359-07) / 1 INSERT in 1 BLISTER PACK (50742-359-03)Marketed from Oct 16, 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): Progesterone
Generic name (nonproprietary): progesterone
Active ingredients: Progesterone — 100 mg/1
Dosage form: Insert
Route: Vaginal
Labeler: Ingenus Pharmaceuticals, LLCNDC labeler code 50742
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 219588
Marketing start: Oct 16, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Progesterone (Chemical structure)
Identifiers: Product ID 50742-359_2b7a32c4-b3ab-46e3-b3c7-bbb2553b8b3aSPL ID 2b7a32c4-b3ab-46e3-b3c7-bbb2553b8b3aSPL set ID abf1bc06-1783-4774-b629-722aa503a898RxCUI 725094UNII 4G7DS2Q64Y
Pharmacologic class: Progesterone

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

N450742035921 followed by a unit qualifier and the quantity

Package 50742-0359-21. 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 Oct 16, 2026.

Indications (excerpt from the label)

Progesterone vaginal insert is indicated, as part of an Assisted Reproductive Technology (ART) treatment program, to support embryo implantation in infertile women less than 35 years of age by supplementation of corpus luteal function and to maintain pregnancy after implantation up to 10 weeks. Progesterone vaginal insert is a progesterone indicated, as part of an Assisted Reproductive Technology (ART) treatment program, to support embryo implantation in infertile women less than 35 years of age by supplementation of corpus luteal function and to maintain pregnancy after implantation up to 10 weeks. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 50742-359

What is NDC 50742-359?: 50742-359 is the product NDC for Progesterone, Progesterone 100 mg/1 insert, listed with the FDA by Ingenus Pharmaceuticals, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Progesterone.
What is the active ingredient?: Progesterone.
Who is the labeler?: Ingenus Pharmaceuticals, LLC, NDC labeler code 50742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Progesterone?: 77 other product NDCs are listed under this name. See all Progesterone 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 Progesterone NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Progesterone	Progesterone 100 mg/1	CapsuleOral	NorthStar Rx LLC	72603-974	72603-0974-01
Progesterone	Progesterone 200 mg/1	CapsuleOral	NorthStar Rx LLC	72603-975	72603-0975-01
Progesterone	Progesterone 100 mg/1	InsertVaginal	Sun Pharmaceutical Industries, Inc.	70095-136	70095-0136-03
Progesterone	Progesterone 100 mg/1	CapsuleOral	Preferred Pharmaceuticals Inc.	68788-4068	68788-4068-03
Progesterone	Progesterone 100 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4552	70518-4552-00
Progesterone	Progesterone 100 mg/1	CapsuleOral	Direct_Rx	72189-654	72189-0654-90
Progesterone	Progesterone 100 mg/1	CapsuleOral	AvKARE	73190-064	73190-0064-01
Progesterone	Progesterone 200 mg/1	CapsuleOral	AvKARE	73190-065	73190-0065-01
Progesterone	Progesterone 200 mg/1	CapsuleOral	Preferred Pharmaceuticals Inc.	68788-4015	68788-4015-03
Progesterone	Progesterone 200 mg/1	CapsuleOral	Hikma Pharmaceuticals USA Inc	0054-0830	00054-0830-25

All 78 Progesterone NDCs