NDC 71335-9609-05 - Omeprazole
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
- 71335-9609
- Requested NDC
- 71335-9609-05
- Package NDCs from labels
- 71335-9609-1, 71335-9609-2, 71335-9609-3, 71335-9609-4, 71335-9609-5, 71335-9609-6, 71335-9609-7, 71335-9609-8, 71335-9609-9, 71335-9609-0, 71335-9609-05
- Manufacturer
- Bryant Ranch Prepack
- Effective date
- 2024-08-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Omeprazole - Bryant Ranch Prepack | Bryant Ranch Prepack | 2024-08-08 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71335-9609-0 | Omeprazole | 7 in 1 BOTTLE | CAPSULE, DELAYED RELEASE | 7 | 104 | |
| 71335-9609-1 | Omeprazole | 30 in 1 BOTTLE | CAPSULE, DELAYED RELEASE | 30 | 104 | |
| 71335-9609-2 | Omeprazole | 60 in 1 BOTTLE | CAPSULE, DELAYED RELEASE | 60 | 104 | |
| 71335-9609-3 | Omeprazole | 56 in 1 BOTTLE | CAPSULE, DELAYED RELEASE | 56 | 104 | |
| 71335-9609-4 | Omeprazole | 90 in 1 BOTTLE | CAPSULE, DELAYED RELEASE | 90 | 104 | |
| 71335-9609-5 | Omeprazole | 20 in 1 BOTTLE | CAPSULE, DELAYED RELEASE | 20 | 104 | |
| 71335-9609-6 | Omeprazole | 15 in 1 BOTTLE | CAPSULE, DELAYED RELEASE | 15 | 104 | |
| 71335-9609-7 | Omeprazole | 120 in 1 BOTTLE | CAPSULE, DELAYED RELEASE | 120 | 104 | |
| 71335-9609-8 | Omeprazole | 100 in 1 BOTTLE | CAPSULE, DELAYED RELEASE | 100 | 104 | |
| 71335-9609-9 | Omeprazole | 28 in 1 BOTTLE | CAPSULE, DELAYED RELEASE | 28 | 104 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 71335-9609 | OMEPRAZOLE CAPSULE, DELAYED RELEASE [BRYANT RANCH PREPACK] | 104 | Current NDC, Legacy NDC, 10 package rows | 20240809_17664f71-154a-47c6-b83c-b349bbc8a98f.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 71335-9609-1 | EA - Each | 71335-9609 | 09f8e273-b14d-4f47-ad0a-106fe8e25367 | 1 | 2023-08-08 |
| 71335-9609-2 | EA - Each | 71335-9609 | 7dde5f6e-b577-4ecd-9b8b-f715c2420394 | 1 | 2023-03-13 |
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 |
|---|---|---|---|---|---|---|
| Stay Ageless Tinted Mineral Sunscreen | BROAD SPECTRUM SPF30 | W Aesthetics | 5b0f2c8f-d6fa-5e25-e063-6394a90a084d | 2026-09-09 | Warnings | 15FIX9V2JP |
| omeprazole | OMEPRAZOLE | Rite Aid Corporation | 28a0b4c8-3ad3-451c-a957-28aef5e3d8b5 | 2026-09-09 | Warnings | KG60484QX9 |
| Omeprazole | OMEPRAZOLE | Amazon.com Services LLC | 94faa721-e925-4033-8661-d1990dfa920d | 2026-08-30 | Warnings | KG60484QX9 |
| Omeprazole | OMEPRAZOLE | REMEDYREPACK INC. | 63b3982a-b541-4b0d-99d4-93a673e57d46 | 2026-08-28 | Warnings, Adverse reactions | 198051 KG60484QX9 |
| MZANK SUNSCREEN DAILY ULTIMATE PROTECTION SPF50 | SUNSCREEN SPF50 | Guangzhou Meixi Biotechnology Co., Ltd. | 5a0b4bd2-f6ad-35dc-e063-6294a90a8a66 | 2026-08-27 | Warnings | 15FIX9V2JP |
| MELAO Hydrating Lightweight Sunscreen | AVOBENZONE,ENSULIZOLE,HOMOSALATE,OCTISALATE,OCTOCRYLENE,TITANIUM DIOXIDE | Guangdong Aimu Biological Technology Co., Ltd | 59eeaea1-d726-99f3-e063-6394a90aeea3 | 2026-08-26 | Warnings | 15FIX9V2JP |
| Q Skin Science | SUNSCREEN | International Cosmeceuticals, Inc | 59e4c3d0-ee4c-2350-e063-6394a90ac9d2 | 2026-08-25 | Warnings | 15FIX9V2JP |
| MELAO zinc stick(GREEN) | TITANIUM DIOXIDE,ZINC OXIDE,OCTOCRYLENE | Guangzhou Haishi Biological Technology Co., Ltd. | 59c70c82-f7ff-9a04-e063-6294a90a7b3d | 2026-08-24 | Warnings | 15FIX9V2JP |
| Smelling Salts | AMMONIA | Shenzhen Finona Information Technology Co., Ltd | 3874ec89-0f1d-87b9-e063-6394a90a300a | 2026-08-24 | Warnings | 5138Q19F1X |
| SKIN-INFUSED FOUNDATION SPF 25/ Mineral sunscreen broad Spectrum SPF 25 01 | ZINC OXIDE, TITANIUM DIOXIDE | Cosmuses Cosmetics (Ningbo) Co., Ltd. | 59d74e3f-e3fa-a7a9-e063-6294a90a76e5 | 2026-08-24 | Warnings | 15FIX9V2JP |
| Rohto Optic Glow | NAPHAZOLINE HYDROCHLORIDE, POVIDONE, PROPYLENE GLYCOL | The Mentholatum Company | df9c5f7c-96e6-4b2b-b8cb-21a6a3342dff | 2026-08-20 | Warnings | 6DC9Q167V3 |
| Smelling Salts | AMMONIA INHALANT, SMELLING SALTS | Hodayfa Abu Alkian | 524e002c-f509-9395-e063-6394a90acd9e | 2026-08-20 | Warnings | 5138Q19F1X |
| Sweat Resistant Sunscreen Body Original | TITANIUM DIOXIDE, ZINC OXIDE | Clutch, Inc. | 4bbde755-e312-123e-e063-6294a90a467f | 2026-08-20 | Warnings | 15FIX9V2JP |
| Smelling Salts | AMMONIA INHALANT, SMELLING SALTS | Shenzhen Leadtop E-commerce Co.,Ltd. | 558e8629-6a8d-198d-e063-6294a90ac5fc | 2026-08-19 | Warnings | 5138Q19F1X |
| omeprazole and sodium bicarbonate | OMEPRAZOLE, SODIUM BICARBONATE | Amazon.com Services LLC | bb453f26-c7df-4cce-8793-337cb5d5f9a9 | 2026-08-19 | Warnings | KG60484QX9 |
| good now omeprazole | OMEPRAZOLE | Gobrands, Inc | 0e7c4aee-2c9f-4d5c-9d47-c333bf00ba9f | 2026-08-19 | Warnings | KG60484QX9 |
| Rohto Preservative Free Dry Aid | POVIDONE, PROPYLENE GLYCOL | The Mentholatum Company | f4b1974c-2412-45f6-b79d-88b8a0bcb608 | 2026-08-18 | Warnings | 6DC9Q167V3 |
| Rohto Dry-Aid | POVIDONE, PROPYLENE GLYCOL | The Mentholatum Company | 8ea5c6c9-48f4-406a-a2cb-9280c546d87d | 2026-08-18 | Warnings | 6DC9Q167V3 |
| Smelling Salt | AMMONIA | Shenzhen Jufeng Qisheng Technology Co., Ltd. | 44e1b2c1-f524-782c-e063-6394a90ad1e4 | 2026-08-18 | Warnings | 5138Q19F1X |
| HEADHUNTER SURF SCREEN SPF 50 SUNSCREEN | ZINC OXIDE,TITANIUM DIOXIDE | Guangzhou Tata Biotechnology Co., Ltd. | 4339df13-77d3-31a1-e063-6394a90a5208 | 2026-08-17 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.