What is NDC 75907-087?

75907-087 is the product NDC for Zovia 1/35 kit, listed with the FDA by Dr. Reddys Laboratories Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Zovia 1/35 (Ethynodiol Diacetate and Ethinyl Estradiol Tablets).

Dr. Reddys Laboratories Inc., NDC labeler code 75907. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Zovia 1/35?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Zovia 1/35 NDC 75907-087 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)75907-087Labeler and product segments. Claims need a package NDC.

Product NDC at billing width75907-0087Add 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
75907-087-28	7590700872875907008728	1 BLISTER PACK in 1 PACKET (75907-087-28) / 1 KIT in 1 BLISTER PACKMarketed from Jun 1, 2024
75907-087-62	7590700876275907008762	6 BLISTER PACK in 1 CARTON (75907-087-62) / 1 KIT in 1 BLISTER PACKMarketed from Jun 1, 2024

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): Zovia 1/35
Generic name (nonproprietary): ethynodiol diacetate and ethinyl estradiol tablets
Dosage form: Kit
Labeler: Dr. Reddys Laboratories Inc.NDC labeler code 75907
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 209548
Marketing start: Jun 1, 2024
Listing expires: Dec 31, 2026
Identifiers: Product ID 75907-087_02181767-b236-4c8f-95b8-00d5e3ef5455SPL ID 02181767-b236-4c8f-95b8-00d5e3ef5455SPL set ID fb636d42-cc1d-47f7-974d-c97c79207f3eRxCUI 310228, 748797, 748804, 748859

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

N475907008728 followed by a unit qualifier and the quantity

Package 75907-0087-28. 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 Jun 1, 2024.

Indications (excerpt from the label)

INDICATIONS AND USAGE Zovia 1/35 is indicated for the prevention of pregnancy in women who elect to use oral contraceptives as a method of contraception. Oral contraceptives are highly effective. Table 1 lists the typical accidental pregnancy rates for users of combination oral contraceptives and other methods of contraception. The efficacy of these contraceptive methods, except sterilization and progestogen implants and injections, depends upon the reliability with which they are used. Correct and consistent use of methods can result in lower failure rates. (A) Among typical couples who initiate use of a method (not necessarily for the first time), the percentage who experience an accidenta…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 75907-087

What is NDC 75907-087?: 75907-087 is the product NDC for Zovia 1/35 kit, listed with the FDA by Dr. Reddys Laboratories Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Zovia 1/35 (Ethynodiol Diacetate and Ethinyl Estradiol Tablets).
Who is the labeler?: Dr. Reddys Laboratories Inc., NDC labeler code 75907. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Zovia 1/35?: 1 other product NDC are listed under this name. See all Zovia 1/35 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 Zovia 1/35 NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Zovia 1/35ethynodiol diacetate and ethinyl estradiol tablets	—	Kit	Mayne Pharma Inc.	51862-894	51862-0894-0151862-0894-03

Other NDCs under ANDA 209548

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

FDA NDC Directory listings under ANDA 209548
Product	Strength	Form · route	Labeler	Product NDC
Zovia 1/35ethynodiol diacetate and ethinyl estradiol tablets	—	Kit	Mayne Pharma Inc.	51862-894