aubra eq

Generic: levonorgestrel and ethinyl estradiol

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name aubra eq
Generic Name levonorgestrel and ethinyl estradiol
Labeler bryant ranch prepack
Dosage Form KIT
Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 63629-5651
Product ID 63629-5651_d8c27882-7acf-4dbe-9e7b-cd25b960bfc6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206886
Listing Expiration 2026-12-31
Marketing Start 2016-11-14

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 636295651
Hyphenated Format 63629-5651

Supplemental Identifiers

RxCUI
242297 748797 748868 1440185

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 aubra eq (source: ndc)
Generic Name levonorgestrel and ethinyl estradiol (source: ndc)
Application Number ANDA206886 (source: ndc)

Resolved Composition

Strengths
  • 0.1 mg/0.02 mg
source: label
Packaging
  • HOW SUPPLIED Aubra EQ® (Levonorgestrel and ethinyl estradiol tablets USP) 0.1 mg/0.02 mg is available in 6 blisterpacks in 1 pouch, each containing 28 tablets: 21 active tablets: White to off-white, round, biconvex, beveled-edge tablets, debossed with “S” on one side and “59” on other side of the tablet. 7 inert tablets: Green, round, mottled, biconvex, beveled-edge uncoated tablets, debossed with “S” on one side and “61” on other side of the tablet. NDC: 63629-5651-1: 6 Blisterpacks in 1 Pouch Store at 20º to 25°C (68° to 77º F) [see USP Controlled Room Temperature]. Repackaged/Relabeled by: Bryant Ranch Prepack, Inc. Burbank, CA 91504
  • Aubra EQ #28 (6x28) Label
source: label

Packages (0)

No package records.

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
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