NDC codes

FDA NDC Directory
Product NDC (as listed)69452-233Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69452-0233Add 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
69452-233-206945202332069452023320100 CAPSULE in 1 BOTTLE (69452-233-20)Marketed from Nov 28, 2018

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
Capsule
Route
Oral
Labeler
Bionpharma Inc.NDC labeler code 69452
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 200900
Marketing start
Listing expires
Other FDA classes
Progesterone (Chemical structure)
Identifiers
Product ID 69452-233_52f7a501-4d23-0fbc-e063-6394a90a4b94SPL ID 52f7a501-4d23-0fbc-e063-6394a90a4b94SPL set ID 41b3c3a7-5fb8-4451-a96c-2bd02613c021RxCUI 260243, 312641UNII 4G7DS2Q64YUPC 0369452234204, 0369452233207
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 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

N469452023320 followed by a unit qualifier and the quantity

Package 69452-0233-20. 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)

INDICATIONS AND USAGE Progesterone capsules are indicated for use in the prevention of endometrial hyperplasia in nonhysterectomized postmenopausal women who are receiving conjugated estrogens tablets. They are also indicated for use in secondary amenorrhea.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 69452-233

What is NDC 69452-233?
69452-233 is the product NDC for Progesterone, Progesterone 100 mg/1 capsule, listed with the FDA by Bionpharma Inc.. 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?
Bionpharma Inc., NDC labeler code 69452. 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?
73 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
ProgesteroneProgesterone 100 mg/1CapsuleOralNorthStar Rx LLC72603-97472603-0974-01
ProgesteroneProgesterone 200 mg/1CapsuleOralNorthStar Rx LLC72603-97572603-0975-01
ProgesteroneProgesterone 100 mg/1InsertVaginalSun Pharmaceutical Industries, Inc.70095-13670095-0136-03
ProgesteroneProgesterone 100 mg/1CapsuleOralPreferred Pharmaceuticals Inc.68788-406868788-4068-03
ProgesteroneProgesterone 100 mg/1CapsuleOralREMEDYREPACK INC.70518-455270518-4552-00
ProgesteroneProgesterone 100 mg/1CapsuleOralDirect_Rx72189-65472189-0654-90
ProgesteroneProgesterone 100 mg/1CapsuleOralAvKARE73190-06473190-0064-01
ProgesteroneProgesterone 200 mg/1CapsuleOralAvKARE73190-06573190-0065-01
ProgesteroneProgesterone 200 mg/1CapsuleOralPreferred Pharmaceuticals Inc.68788-401568788-4015-03
ProgesteroneProgesterone 100 mg/1CapsuleOralHikma Pharmaceuticals USA Inc0054-082900054-0829-25

All 74 Progesterone NDCs

Other NDCs under ANDA 200900

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

FDA NDC Directory listings under ANDA 200900
ProductStrengthForm · routeLabelerProduct NDC
ProgesteroneProgesterone 100 mg/1CapsuleOralA-S Medication Solutions50090-6771
ProgesteroneProgesterone 100 mg/1CapsuleOralGolden State Medical Supply, Inc.51407-980
ProgesteroneProgesterone 200 mg/1CapsuleOralGolden State Medical Supply, Inc.51407-981
ProgesteroneProgesterone 100 mg/1CapsuleOralBryant Ranch Prepack71335-9739
ProgesteroneProgesterone 100 mg/1CapsuleOralBionpharma Inc.69452-148
ProgesteroneProgesterone 200 mg/1CapsuleOralBionpharma Inc.69452-149
ProgesteroneProgesterone 200 mg/1CapsuleOralBionpharma Inc.69452-234
ProgesteroneProgesterone 100 mg/1CapsuleOralPreferred Pharmaceuticals Inc.68788-8709
ProgesteroneProgesterone 200 mg/1CapsuleOralNuCare Pharmaceuticals,Inc.68071-3529
ProgesteroneProgesterone 200 mg/1CapsuleOralPreferred Pharmaceuticals Inc.68788-8719
ProgesteroneProgesterone 200 mg/1CapsuleOralBryant Ranch Prepack71335-2242
ProgesteroneProgesterone 100 mg/1CapsuleOralNuCare Pharmaceuticals,Inc.68071-3557
ProgesteroneProgesterone 200 mg/1CapsuleOralProficient Rx LP82804-268
ProgesteroneProgesterone 100 mg/1CapsuleOralREMEDYREPACK INC.70518-4166
ProgesteroneProgesterone 200 mg/1CapsuleOralAsclemed USA, Inc.76420-580
ProgesteroneProgesterone 100 mg/1CapsuleOralAsclemed USA, Inc.76420-582

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