NDC codes

FDA NDC Directory
Product NDC (as listed)70700-116Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70700-0116Add 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
70700-116-8570700011685707000116853 BLISTER PACK in 1 CARTON (70700-116-85) / 1 KIT in 1 BLISTER PACKMarketed from Mar 2, 2023

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)
Altavera
Generic name (nonproprietary)
levonorgestrel and ethinyl estradiol
Dosage form
Kit
Labeler
Xiromed, LLC.NDC labeler code 70700
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 079102
Marketing start
Listing expires
Identifiers
Product ID 70700-116_cd0fbf86-78dd-a8f2-7399-112a042ab767SPL ID cd0fbf86-78dd-a8f2-7399-112a042ab767SPL set ID 4701e72b-6378-a771-fb88-1b703031a8bcRxCUI 238019, 748797, 748878, 1006065UPC 0370700116852

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.

NDC on a medical claim

N470700011685 followed by a unit qualifier and the quantity

Package 70700-0116-85. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Altavera is indicated for use by females of reproductive potential to prevent pregnancy.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70700-116

What is NDC 70700-116?
70700-116 is the product NDC for Altavera kit, listed with the FDA by Xiromed, LLC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Altavera (Levonorgestrel and Ethinyl Estradiol).
Who is the labeler?
Xiromed, LLC., NDC labeler code 70700. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Altavera?
1 other product NDC are listed under this name. See all Altavera 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 Altavera NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Altaveralevonorgestrel and ethinyl estradiol—KitBryant Ranch Prepack63629-234363629-2343-01

Other NDCs under ANDA 079102

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

FDA NDC Directory listings under ANDA 079102
ProductStrengthForm · routeLabelerProduct NDC
Altaveralevonorgestrel and ethinyl estradiol—KitBryant Ranch Prepack63629-2343

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