What is NDC 70771-1988?

70771-1988 is the product NDC for Ammonium lactate, Ammonium lactate 120 mg/g cream, 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 Ammonium lactate?

13 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Ammonium lactate NDC 70771-1988 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70771-1988Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70771-1988Add 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
70771-1988-6	7077119880670771198806	2 TUBE in 1 CARTON (70771-1988-6) / 140 g in 1 TUBE (70771-1988-5)Marketed from Oct 2, 2026
70771-1988-7	7077119880770771198807	385 g in 1 BOTTLE (70771-1988-7)Marketed from Oct 2, 2026

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): Ammonium lactate
Generic name (nonproprietary): ammonium lactate
Active ingredients: Ammonium lactate — 120 mg/g
Dosage form: Cream
Route: Topical
Labeler: Zydus Lifesciences LimitedNDC labeler code 70771
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217815
Marketing start: Oct 2, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Acidifying Activity (Mechanism)
Identifiers: Product ID 70771-1988_2fba2d8c-f152-49fd-88bf-2cec6a189264SPL ID 2fba2d8c-f152-49fd-88bf-2cec6a189264SPL set ID 10a894e6-d23a-4142-8c9f-7bf96be9b991UNII 67M901L9NQ

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

N470771198806 followed by a unit qualifier and the quantity

Package 70771-1988-06. 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 2, 2026.

Full label on DailyMed (opens in a new tab)

About NDC 70771-1988

What is NDC 70771-1988?: 70771-1988 is the product NDC for Ammonium lactate, Ammonium lactate 120 mg/g cream, 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?: Ammonium lactate.
What is the active ingredient?: Ammonium lactate.
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 Ammonium lactate?: 13 other product NDCs are listed under this name. See all Ammonium lactate 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 Ammonium lactate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Ammonium lactate	Ammonium lactate 120 mg/g	CreamTopical	Viona Pharmaceuticals Inc	72578-203	72578-0203-1072578-0203-11
Ammonium Lactate	Ammonium lactate 120 mg/g	CreamTopical	REMEDYREPACK INC.	70518-3619	70518-3619-00
Ammonium Lactate	Ammonium lactate 12 g/100g	CreamTopical	Padagis Israel Pharmaceuticals Ltd	45802-493	45802-0493-2645802-0493-38
Ammonium Lactate	Ammonium lactate 12 g/100g	CreamTopical	Bryant Ranch Prepack	63629-8608	63629-8608-01
Ammonium Lactate	Ammonium lactate 12 g/100g	CreamTopical	Bryant Ranch Prepack	63629-8609	63629-8609-01
Ammonium Lactate	Ammonium lactate 12 g/100g	CreamTopical	Bryant Ranch Prepack	72162-1413	72162-1413-02
Ammonium Lactate	Ammonium lactate 12 g/100g	LotionTopical	Padagis Israel Pharmaceuticals Ltd	45802-419	45802-0419-2645802-0419-54
Ammonium Lactate	Ammonium lactate 12 g/100g	LotionTopical	Bryant Ranch Prepack	63629-8610	63629-8610-01
Ammonium Lactate	Ammonium lactate 12 g/100g	LotionTopical	Bryant Ranch Prepack	63629-8611	63629-8611-01
Ammonium Lactate	Ammonium lactate 12 g/100g	LotionTopical	Bryant Ranch Prepack	72162-1407	72162-1407-0272162-1407-04

All 14 Ammonium lactate NDCs

Other NDCs under ANDA 217815

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

FDA NDC Directory listings under ANDA 217815
Product	Strength	Form · route	Labeler	Product NDC
Ammonium lactate	Ammonium lactate 120 mg/g	CreamTopical	Viona Pharmaceuticals Inc	72578-203