NDC 71335-1010-01 - Atorvastatin Calcium
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 71335-1010
- Requested NDC
- 71335-1010-01
- Package NDCs from labels
- 71335-1010-1, 71335-1010-2, 71335-1010-3, 71335-1010-4, 71335-1010-5, 71335-1010-6, 71335-1010-7, 71335-1010-8, 71335-1010-9, 71335-1010-01
- Manufacturer
- Bryant Ranch Prepack
- Effective date
- 2024-05-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Atorvastatin Calcium - Bryant Ranch Prepack | Bryant Ranch Prepack | 2024-05-30 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71335-1010-1 | Atorvastatin Calcium | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | 13 | |
| 71335-1010-2 | Atorvastatin Calcium | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | 13 | |
| 71335-1010-3 | Atorvastatin Calcium | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | 13 | |
| 71335-1010-4 | Atorvastatin Calcium | 9 in 1 BOTTLE | TABLET, FILM COATED | 9 | 13 | |
| 71335-1010-5 | Atorvastatin Calcium | 28 in 1 BOTTLE | TABLET, FILM COATED | 28 | 13 | |
| 71335-1010-6 | Atorvastatin Calcium | 20 in 1 BOTTLE | TABLET, FILM COATED | 20 | 13 | |
| 71335-1010-7 | Atorvastatin Calcium | 180 in 1 BOTTLE | TABLET, FILM COATED | 180 | 13 | |
| 71335-1010-8 | Atorvastatin Calcium | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | 13 | |
| 71335-1010-9 | Atorvastatin Calcium | 7 in 1 BOTTLE | TABLET, FILM COATED | 7 | 13 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 71335-1010 | ATORVASTATIN CALCIUM TABLET, FILM COATED [BRYANT RANCH PREPACK] | 13 | Current NDC, Legacy NDC, 9 package rows | 20240601_bbb1a527-3b4d-4fd4-9e38-b231ad5d6d8f.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 71335-1010-1 | EA - Each | 71335-1010 | 280f2acd-fbe8-4dd5-9186-f47c52c512f9 | 1 | 2020-09-14 |
| 71335-1010-3 | EA - Each | 71335-1010 | cc19ee05-ab01-458b-8b42-9d683be679bc | 1 | 2020-09-14 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Atorvastatin calcium | ATORVASTATIN CALCIUM | REMEDYREPACK INC. | 5b3c3043-9af6-48eb-8b10-528e58c88e48 | 2026-08-06 | Warnings, Adverse reactions | 48A5M73Z4Q |
| Atorvastatin calcium | ATORVASTATIN CALCIUM | REMEDYREPACK INC. | 51e24220-3374-4e5e-9a8d-4113002c5bed | 2026-08-06 | Warnings, Adverse reactions | 48A5M73Z4Q |
| Atorvastatin calcium | ATORVASTATIN CALCIUM | REMEDYREPACK INC. | b0bbab86-6789-4ffb-8f84-ee91b69fdb34 | 2026-08-06 | Warnings, Adverse reactions | 617310 48A5M73Z4Q |
| AMAZON EXTRA STRENGTH | SIMETHICONE | AMAZON.COM SERVICES LLC | 705489ce-ac7c-44a8-8298-ead19824582e | 2026-08-06 | Warnings | 92RU3N3Y1O |
| EltaMD UV Restore | TITANIUM DIOXIDE, ZINC OXIDE SUNSCREEN | CP Skin Health Group, Inc | 37fee381-ce6b-4949-9a4a-778aa839fb84 | 2026-08-06 | Warnings | 15FIX9V2JP |
| Atorvastatin calcium | ATORVASTATIN CALCIUM | REMEDYREPACK INC. | 9786388d-ac8d-4646-9fe4-b33e8fda86b2 | 2026-08-05 | Warnings, Adverse reactions | 48A5M73Z4Q |
| Gencare-Gas Relief | SIMETHICONE 180 MG | PIONEER LIFE SCIENCES, LLC | b7f2d5db-c1b7-4c01-8ee6-017e4b9f1425 | 2026-08-04 | Warnings | 92RU3N3Y1O |
| Luxe Gloss Hydrating Lip Gloss SPF 35-NAKED HONEY | OCTOCRYLENE 8%, OCTISALATE 5%, TITANIUM DIOXIDE 6%, ZINC OXIDE 8% | Lale Cosmetics LLC | 581fb0cd-c55d-d562-e063-6394a90a7f11 | 2026-08-03 | Warnings | 15FIX9V2JP |
| EltaMD UV Active | ZINC OXIDE AND TITANIUM DIOXIDE SUNSCREEN | CP Skin Health Group, Inc | 39d16479-d491-4c19-aa11-674461687c7b | 2026-08-03 | Warnings | 15FIX9V2JP |
| Simethicone | SIMETHICONE | Aphena Pharma Solutions - Tennessee, LLC | da0cc98e-1692-405a-ab81-420d6f9df6de | 2026-07-31 | Warnings | 92RU3N3Y1O |
| Atorvastatin Calcium | ATORVASTATIN CALCIUM | REMEDYREPACK INC. | 09cb8375-075c-47e8-a4eb-8ac667ed849e | 2026-07-31 | Warnings, Adverse reactions | 617310 48A5M73Z4Q |
| Continuous Correction Cream | TITANIUM DIOXIDE | Baxter of California, LLC | 1cbcc648-f2e1-af60-e063-6294a90ad4bb | 2026-07-31 | Warnings | 15FIX9V2JP |
| Cover Creme | TITANIUM DIOXIDE | Baxter of California | 31f5e8c4-523f-4596-e063-6294a90a6a12 | 2026-07-31 | Warnings | 15FIX9V2JP |
| INFANTS GAS RELIEF DROPS | SIMETHICONE | RELIABLE 1 LABORATORIES | b479bf22-3469-7916-e053-2995a90addc8 | 2026-07-30 | Warnings | 92RU3N3Y1O |
| Atorvastatin Calcium | ATORVASTATIN CALCIUM | Cardinal Health 107, LLC | aee307d6-b3fa-424f-8656-1f30ff413e95 | 2026-07-30 | Warnings, Adverse reactions | 48A5M73Z4Q |
| DUAL ACTION COMPLETE | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | Amazon.com Services LLC | 4e8a936c-b876-4923-ad9e-d23537b5d7cf | 2026-07-28 | Warnings | H0G9379FGK |
| TUMS ULTRA | CALCIUM CARBONATE | Haleon US Holdings LLC | 348d3dfa-6a52-4583-96e3-83c4bf2df45b | 2026-07-27 | Warnings | H0G9379FGK |
| Pepcid Complete | FAMOTIDINE, CALCIUM CARBONATE, AND MAGNESIUM HYDROXIDE | Kenvue Brands LLC | a2ef8424-7d80-42b0-a01e-f378f629b2b6 | 2026-07-24 | Warnings | H0G9379FGK |
| Gethorey Vein Target Microneedle Patch | ALLANTOIN 2% VEIN TARGET MICRONEEDLE PATCH | Wenzhou Yuyuan Pharmaceutical Co., Ltd. | 57593145-a874-15d9-e063-6294a90a77d9 | 2026-07-24 | Warnings | 92RU3N3Y1O |
| ESIKA COLORFIX POLVOS 32H POLVO COMPACTO FACIAL DE ALTA COBERTURA FPS 15 110-C | OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE | BEL STAR S.A. | 575fb2c3-e332-8a3b-e063-6394a90a9fd9 | 2026-07-24 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.