Betamethasone dipropionate NDC 70771-1380

NDC codes

FDA NDC Directory

Product NDC (as listed)70771-1380Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70771-1380Add 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
70771-1380-1	70771138001	1 TUBE in 1 CARTON (70771-1380-1) / 15 g in 1 TUBEMarketed from Feb 26, 2019
70771-1380-4	70771138004	1 TUBE in 1 CARTON (70771-1380-4) / 45 g in 1 TUBEMarketed from Feb 26, 2019

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): Betamethasone dipropionate
Generic name (nonproprietary): betamethasone dipropionate
Active ingredients: Betamethasone dipropionate — .5 mg/g
Dosage form: Cream
Route: Topical
Labeler: Zydus Lifesciences Limited
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 208885
Marketing start: Feb 26, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 70771-1380_02c750ed-2344-42d0-bfb8-4729f197ed99SPL ID 02c750ed-2344-42d0-bfb8-4729f197ed99SPL set ID bc9ca1f4-8f40-44e1-bb2d-42ecba35d406RxCUI 238920UNII 826Y60901U
Pharmacologic class: Corticosteroid

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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N470771138001 followed by a unit qualifier and the quantity

Package 70771-1380-01. 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 Nov 25, 2024.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 208885

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

FDA NDC Directory listings under ANDA 208885
Product	Strength	Form · route	Labeler	Product NDC
Betamethasone dipropionate	Betamethasone dipropionate .5 mg/g	CreamTopical	A-S Medication Solutions	50090-4680
Betamethasone dipropionate	Betamethasone dipropionate .5 mg/g	CreamTopical	Zydus Pharmaceuticals USA Inc.	70710-1233
Betamethasone dipropionate	Betamethasone dipropionate .5 mg/g	CreamTopical	Northstar Rx LLC.	16714-996
Betamethasone dipropionate	Betamethasone dipropionate .5 mg/g	CreamTopical	Redpharm Drug	67296-2275
Betamethasone dipropionate	Betamethasone dipropionate .5 mg/g	CreamTopical	A-S Medication Solutions	50090-7525