altavera

Generic: levonorgestrel and ethinyl estradiol

Labeler: xiromed, llc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name altavera
Generic Name levonorgestrel and ethinyl estradiol
Labeler xiromed, llc.
Dosage Form KIT
Manufacturer
Xiromed, LLC.

Identifiers & Regulatory

Product NDC 70700-116
Product ID 70700-116_cd0fbf86-78dd-a8f2-7399-112a042ab767
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA079102
Listing Expiration 2026-12-31
Marketing Start 2022-09-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70700116
Hyphenated Format 70700-116

Supplemental Identifiers

RxCUI
238019 748797 748878 1006065
UPC
0370700116852

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name altavera (source: ndc)
Generic Name levonorgestrel and ethinyl estradiol (source: ndc)
Application Number ANDA079102 (source: ndc)

Resolved Composition

Strengths
  • 0.15 mg/30 mcg
source: label
Packaging
  • 3 BLISTER PACK in 1 CARTON (70700-116-85) / 1 KIT in 1 BLISTER PACK
source: ndc

Packages (1)

70700-116-85 3 BLISTER PACK in 1 CARTON (70700-116-85) / 1 KIT in 1 BLISTER PACK

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

ALTAVERA ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "cd0fbf86-78dd-a8f2-7399-112a042ab767", "openfda": {"upc": ["0370700116852"], "rxcui": ["238019", "748797", "748878", "1006065"], "spl_set_id": ["4701e72b-6378-a771-fb88-1b703031a8bc"], "manufacturer_name": ["Xiromed, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (70700-116-85)  / 1 KIT in 1 BLISTER PACK", "package_ndc": "70700-116-85", "marketing_start_date": "20230302"}], "brand_name": "ALTAVERA", "product_id": "70700-116_cd0fbf86-78dd-a8f2-7399-112a042ab767", "dosage_form": "KIT", "product_ndc": "70700-116", "generic_name": "Levonorgestrel and Ethinyl Estradiol", "labeler_name": "Xiromed, LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ALTAVERA", "application_number": "ANDA079102", "marketing_category": "ANDA", "marketing_start_date": "20220901", "listing_expiration_date": "20261231"}