NDC codes

FDA NDC Directory
Product NDC (as listed)70095-136Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70095-0136Add 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
70095-136-03700950136031 CARTON in 1 CARTON (70095-136-03) / 21 BLISTER PACK in 1 CARTON (70095-136-02) / 1 INSERT in 1 BLISTER PACK (70095-136-01)Marketed from Apr 27, 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
Product type
Prescription drug
Marketing category
NDA authorized genericApplication NDA 022057
Marketing start
Listing expires
Other FDA classes
Progesterone (Chemical structure)
Identifiers
Product ID 70095-136_5232dd12-1767-7fa2-e063-6294a90a4e70SPL ID 5232dd12-1767-7fa2-e063-6294a90a4e70SPL set ID fcdde0d0-4329-4725-a76b-684f9d97fe95RxCUI 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

N470095013603 followed by a unit qualifier and the quantity

Package 70095-0136-03. 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)

Progesterone vaginal insert is indicated to support embryo implantation and early pregnancy by supplementation of corpus luteal function as part of an Assisted Reproductive Technology (ART) treatment program for infertile women. Progesterone vaginal insert is a progesterone indicated to support embryo implantation and early pregnancy by supplementation of corpus luteal function as part of an Assisted Reproductive Technology (ART) treatment program for infertile women. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under NDA 022057

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

FDA NDC Directory listings under NDA 022057
ProductStrengthForm · routeLabelerProduct NDC
EndometrinprogesteroneProgesterone 100 mg/1InsertVaginalFerring Pharmaceuticals Inc.55566-6500

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