What is NDC 70121-1686?

70121-1686 is the product NDC for Exenatide, Exenatide 250 ug/mL injection, listed with the FDA by Amneal Pharmaceuticals LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Amneal Pharmaceuticals LLC, NDC labeler code 70121. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Exenatide?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Exenatide NDC 70121-1686 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70121-1686Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70121-1686Add 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
70121-1686-1	70121168601	1 CARTRIDGE in 1 CARTON (70121-1686-1) / 2.4 mL in 1 CARTRIDGEMarketed from Nov 22, 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): Exenatide
Generic name (nonproprietary): exenatide
Active ingredients: Exenatide — 250 ug/mL
Dosage form: Injection
Route: Subcutaneous
Labeler: Amneal Pharmaceuticals LLCNDC labeler code 70121
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 206697
Marketing start: Nov 22, 2024
Marketing end: May 31, 2027
Other FDA classes: Glucagon-Like Peptide 1 (Chemical structure)Glucagon-like Peptide-1 (GLP-1) Agonists (Mechanism)
Identifiers: Product ID 70121-1686_2141c3ca-074a-4098-85da-1ef78ec4d4dcSPL ID 2141c3ca-074a-4098-85da-1ef78ec4d4dcSPL set ID e6cb5c8f-e97f-4a6a-95a4-939fd2393949RxCUI 847910, 847915UNII 9P1872D4OL
Pharmacologic class: GLP-1 Receptor Agonist

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

Administration

Drug administration (CPT 96360–96549)

When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.

How CPT relates to drug billing

NDC on a medical claim

N470121168601 followed by a unit qualifier and the quantity

Package 70121-1686-01. 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 May 27, 2026.

Indications (excerpt from the label)

Exenatide injection is indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. Exenatide injection is a glucagon-like peptide-1 (GLP-1) receptor agonist indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. ( 1 , 14 ) Limitations of Use Co-administration with other exenatide-containing products is not recommended. ( 1 ) Limitations of Use Exenatide injection contains exenatide. Co-administration with other exenatide-containing products is not recommended.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70121-1686

What is NDC 70121-1686?: 70121-1686 is the product NDC for Exenatide, Exenatide 250 ug/mL injection, listed with the FDA by Amneal Pharmaceuticals LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Exenatide.
What is the active ingredient?: Exenatide.
Who is the labeler?: Amneal Pharmaceuticals LLC, NDC labeler code 70121. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Exenatide?: 1 other product NDC are listed under this name. See all Exenatide 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 Exenatide NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Exenatide	Exenatide 250 ug/mL	InjectionSubcutaneous	Amneal Pharmaceuticals LLC	70121-1685	70121-1685-01

Other NDCs under ANDA 206697

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

FDA NDC Directory listings under ANDA 206697
Product	Strength	Form · route	Labeler	Product NDC
Exenatide	Exenatide 250 ug/mL	InjectionSubcutaneous	Amneal Pharmaceuticals LLC	70121-1685