NDC codes

FDA NDC Directory
Product NDC (as listed)81033-150Labeler and product segments. Claims need a package NDC.
Product NDC at billing width81033-0150Add 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
81033-150-43810330150438103301504330 CUP, UNIT-DOSE in 1 CARTON (81033-150-43) / 20 mL in 1 CUP, UNIT-DOSE (81033-150-20)Marketed from Aug 7, 2025
81033-150-44810330150448103301504440 CUP, UNIT-DOSE in 1 CARTON (81033-150-44) / 10 mL in 1 CUP, UNIT-DOSE (81033-150-10)Marketed from Aug 7, 2025
81033-150-528103301505281033015052100 CUP, UNIT-DOSE in 1 CASE (81033-150-52) / 10 mL in 1 CUP, UNIT-DOSE (81033-150-10)Marketed from Aug 7, 2025

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)
Megestrol Acetate
Generic name (nonproprietary)
megestrol acetate
Active ingredients
Megestrol acetate — 40 mg/mL
Dosage form
Suspension
Route
Oral
Labeler
Kesin Pharma CorporationNDC labeler code 81033
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 075671
Marketing start
Listing expires
Other FDA classes
Progesterone Congeners (Chemical structure)
Identifiers
Product ID 81033-150_3dd3d565-dc60-0c31-e063-6394a90a46e3SPL ID 3dd3d565-dc60-0c31-e063-6394a90a46e3SPL set ID 3bc8708e-a52d-fda2-e063-6294a90a0fbcRxCUI 860225UNII TJ2M0FR8ES
Pharmacologic class
Progestin

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

N481033015043 followed by a unit qualifier and the quantity

Package 81033-0150-43. 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 Megestrol acetate oral suspension, USP is indicated for the treatment of anorexia, cachexia, or an unexplained, significant weight loss in patients with a diagnosis of acquired immunodeficiency syndrome (AIDS).

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 81033-150

What is NDC 81033-150?
81033-150 is the product NDC for Megestrol Acetate, Megestrol acetate 40 mg/mL suspension, listed with the FDA by Kesin Pharma Corporation. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Megestrol Acetate.
What is the active ingredient?
Megestrol acetate.
Who is the labeler?
Kesin Pharma Corporation, NDC labeler code 81033. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Megestrol Acetate?
23 other product NDCs are listed under this name. See all Megestrol Acetate 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 Megestrol Acetate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Megestrol AcetateMegestrol acetate 20 mg/1TabletOralREMEDYREPACK INC.70518-464070518-4640-00
Megestrol AcetateMegestrol acetate 40 mg/mLSuspensionOralAmerican Health Packaging60687-91660687-0916-0860687-0916-56
Megestrol AcetateMegestrol acetate 400 mg/10mLSuspensionOralMajor Pharmaceuticals0904-757700904-7577-1800904-7577-72
Megestrol AcetateMegestrol acetate 400 mg/10mLSuspensionOralPAI Holdings, LLC dba PAI Pharma0121-103800121-1038-0000121-1038-40
Megestrol AcetateMegestrol acetate 40 mg/mLSuspensionOralXttrium Laboratories, Inc.0116-401100116-4011-0800116-4011-1100116-4011-16+2 more
Megestrol AcetateMegestrol acetate 40 mg/mLSuspensionOralPreferred Pharmaceuticals Inc.68788-871468788-8714-02
Megestrol AcetateMegestrol acetate 40 mg/mLSuspensionOralANI Pharmaceuticals, Inc.70954-89670954-0896-1070954-0896-20
Megestrol AcetateMegestrol acetate 40 mg/mLSuspensionOralNatco Pharma USA LLC69339-16069339-0160-1669339-0160-1769339-0160-18+1 more
Megestrol AcetateMegestrol acetate 40 mg/mLSuspensionOralPrecision Dose Inc.68094-06368094-0063-6168094-0063-62
Megestrol AcetateMegestrol acetate 40 mg/mLSuspensionOralPrecision Dose Inc.68094-17468094-0174-62

All 24 Megestrol Acetate NDCs

Other NDCs under ANDA 075671

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

FDA NDC Directory listings under ANDA 075671
ProductStrengthForm · routeLabelerProduct NDC
Megestrol AcetateMegestrol acetate 400 mg/10mLSuspensionOralPAI Holdings, LLC dba PAI Pharma0121-0945
Megestrol AcetateMegestrol acetate 40 mg/mLSuspensionOralATLANTIC BIOLOGICALS CORP.17856-0060
Megestrol AcetateMegestrol acetate 40 mg/mLSuspensionOralGolden State Medical Supply, Inc.51407-910
Megestrol AcetateMegestrol acetate 40 mg/mLSuspensionOralStrides Pharma Science Limited64380-160
Megestrol AcetateMegestrol acetate 40 mg/mLSuspensionOralPrecision Dose Inc.68094-063
Megestrol AcetateMegestrol acetate 40 mg/mLSuspensionOralPrecision Dose Inc.68094-174
Megestrol AcetateMegestrol acetate 40 mg/mLSuspensionOralPreferred Pharmaceuticals Inc.68788-8714
Megestrol AcetateMegestrol acetate 40 mg/mLSuspensionOralNatco Pharma USA LLC69339-160

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