What is NDC 70771-1893?

70771-1893 is the product NDC for Fludrocortisone acetate, Fludrocortisone acetate .1 mg/1 tablet, listed with the FDA by Zydus Lifesciences Limited. It has 2 package NDCs, shown above in 10- and 11-digit form.

Zydus Lifesciences Limited, NDC labeler code 70771. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Fludrocortisone acetate?

15 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Fludrocortisone acetate NDC 70771-1893

NDC codes

FDA NDC Directory

Product NDC (as listed)70771-1893Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70771-1893Add 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
70771-1893-1	70771189301	100 TABLET in 1 BOTTLE (70771-1893-1)Marketed from Dec 2, 2024
70771-1893-5	70771189305	500 TABLET in 1 BOTTLE (70771-1893-5)Marketed from Dec 2, 2024

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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): Fludrocortisone acetate
Generic name (nonproprietary): fludrocortisone acetate
Active ingredients: Fludrocortisone acetate — .1 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Zydus Lifesciences LimitedNDC labeler code 70771
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 219251
Marketing start: Dec 2, 2024
Listing expires: Dec 31, 2026
Identifiers: Product ID 70771-1893_3d915d99-8d45-4077-990f-da0f653675a2SPL ID 3d915d99-8d45-4077-990f-da0f653675a2SPL set ID 6c4a7d2d-00a4-4d80-ab4c-2afd4e4f614eRxCUI 313979UNII V47IF0PVH4

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

N470771189301 followed by a unit qualifier and the quantity

Package 70771-1893-01. 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 Oct 29, 2024.

Indications (excerpt from the label)

INDICATIONS AND USAGE Fludrocortisone acetate tablets are indicated as partial replacement therapy for primary and secondary adrenocortical insufficiency in Addison's disease and for the treatment of salt-losing adrenogenital syndrome.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70771-1893

What is NDC 70771-1893?: 70771-1893 is the product NDC for Fludrocortisone acetate, Fludrocortisone acetate .1 mg/1 tablet, listed with the FDA by Zydus Lifesciences Limited. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Fludrocortisone acetate.
What is the active ingredient?: Fludrocortisone acetate.
Who is the labeler?: Zydus Lifesciences Limited, NDC labeler code 70771. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Fludrocortisone acetate?: 15 other product NDCs are listed under this name. See all Fludrocortisone 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 Fludrocortisone acetate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
fludrocortisone acetate	Fludrocortisone acetate .1 mg/1	TabletOral	Eywa Pharma Inc	71930-088	71930-0088-1271930-0088-52
Fludrocortisone Acetate	Fludrocortisone acetate .1 mg/1	TabletOral	Cardinal Health 107, LLC	55154-2644	55154-2644-00
Fludrocortisone acetate	Fludrocortisone acetate .1 mg/1	TabletOral	Viona Pharmaceuticals Inc	72578-164	72578-0164-0172578-0164-05
Fludrocortisone acetate	Fludrocortisone acetate .1 mg/1	TabletOral	Golden State Medical Supply, Inc.	51407-705	51407-0705-01
Fludrocortisone Acetate	Fludrocortisone acetate .1 mg/1	TabletOral	Major Pharmaceuticals	0904-7317	00904-7317-0600904-7317-61
Fludrocortisone Acetate	Fludrocortisone acetate .1 mg/1	TabletOral	NorthStar Rx LLC	72603-170	72603-0170-01
Fludrocortisone Acetate	Fludrocortisone acetate .1 mg/1	TabletOral	Novitium Pharma LLC	70954-252	70954-0252-1070954-0252-2070954-0252-30
Fludrocortisone Acetate	Fludrocortisone acetate .1 mg/1	TabletOral	Bryant Ranch Prepack	71335-2454	71335-2454-01
Fludrocortisone Acetate	Fludrocortisone acetate .1 mg/1	TabletOral	AvKARE	42291-764	42291-0764-01
Fludrocortisone Acetate	Fludrocortisone acetate .1 mg/1	TabletOral	AvPAK	50268-330	50268-0330-15

All 16 Fludrocortisone acetate NDCs

Other NDCs under ANDA 219251

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

FDA NDC Directory listings under ANDA 219251
Product	Strength	Form · route	Labeler	Product NDC
Fludrocortisone acetate	Fludrocortisone acetate .1 mg/1	TabletOral	Golden State Medical Supply, Inc.	51407-705
Fludrocortisone acetate	Fludrocortisone acetate .1 mg/1	TabletOral	Viona Pharmaceuticals Inc	72578-164