NDC 70518-2604-05 - Sulfamethoxazole and Trimethoprim
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
- 70518-2604
- Requested NDC
- 70518-2604-05
- Package NDCs from labels
- 70518-2604-0, 70518-2604-1, 70518-2604-2, 70518-2604-3, 70518-2604-4, 70518-2604-5, 70518-2604-6, 70518-2604-7, 70518-2604-8, 70518-2604-9, 70518-2604-05
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2026-07-27
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Sulfamethoxazole and Trimethoprim Tablets, USP | REMEDYREPACK INC. | 2026-07-27 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70518-2604-0 | Sulfamethoxazole and Trimethoprim | 14 in 1 BOTTLE, PLASTIC | TABLET | 14 | 25 | |
| 70518-2604-1 | Sulfamethoxazole and Trimethoprim | 20 in 1 BOTTLE, PLASTIC | TABLET | 20 | 25 | |
| 70518-2604-2 | Sulfamethoxazole and Trimethoprim | 6 in 1 BOTTLE, PLASTIC | TABLET | 6 | 25 | |
| 70518-2604-3 | Sulfamethoxazole and Trimethoprim | 14 in 1 BLISTER PACK | TABLET | 14 | 25 | |
| 70518-2604-4 | Sulfamethoxazole and Trimethoprim | 20 in 1 BOTTLE, PLASTIC | TABLET | 20 | 25 | |
| 70518-2604-5 | Sulfamethoxazole and Trimethoprim | 30 in 1 BLISTER PACK | TABLET | 30 | 25 | |
| 70518-2604-6 | Sulfamethoxazole and Trimethoprim | 20 in 1 BLISTER PACK | TABLET | 20 | 25 | |
| 70518-2604-7 | Sulfamethoxazole and Trimethoprim | 21 in 1 BOTTLE, PLASTIC | TABLET | 21 | 25 | |
| 70518-2604-8 | Sulfamethoxazole and Trimethoprim | 14 in 1 BOTTLE, PLASTIC | TABLET | 14 | 25 | |
| 70518-2604-9 | Sulfamethoxazole and Trimethoprim | 10 in 1 BOTTLE, PLASTIC | TABLET | 10 | 25 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70518-2604 | SULFAMETHOXAZOLE AND TRIMETHOPRIM TABLET [REMEDYREPACK INC.] | 22 | Current NDC, Legacy NDC, 10 package rows | 20250202_c45ac3a4-d397-486e-abd1-349916543068.zip |
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 |
|---|---|---|---|---|---|---|
| polymyxin b sulfate and trimethoprim sulfate | POLYMYXIN B SULFATE AND TRIMETHOPRIM SULFATE | REMEDYREPACK INC. | c68818b2-d849-41d2-be07-731244afbbac | 2026-09-09 | Warnings, Adverse reactions | AN164J8Y0X |
| Stool Softener Laxative | DOCUSATE SODIUM | TARGET Corporation | 4180a35b-cc50-46ae-a100-99bb218c10ff | 2026-09-09 | Warnings | F05Q2T2JA0 |
| SULFATRIM | SULFAMETHOXAZOLE AND TRIMETHOPRIM | Preferred Pharmaceuticals, Inc. | cd4932ce-0856-4e99-8baf-70afce1d7ffd | 2026-09-02 | Warnings, Adverse reactions | AN164J8Y0X JE42381TNV |
| Sulfamethoxazole and Trimethoprim | SULFAMETHOXAZOLE AND TRIMETHOPRIM | Preferred Pharmaceuticals Inc. | d60c218c-6529-4944-af0b-a9dc720f32e9 | 2026-09-02 | Warnings, Adverse reactions | ANDA090624 198335 AN164J8Y0X JE42381TNV |
| Kroger Stool Softener Fruit Punch | DOCUSATE SODIUM | KROGER COMPANY | b86f8f3d-594e-466c-854a-b8bff9f7a0b8 | 2026-09-02 | Warnings | F05Q2T2JA0 |
| Sulfamethoxazole and Trimethoprim | SULFAMETHOXAZOLE AND TRIMETHOPRIM | Preferred Pharmaceuticals Inc. | c6171b62-835c-465e-905e-97f70438186e | 2026-09-02 | Warnings, Adverse reactions | AN164J8Y0X JE42381TNV |
| Stimulant Laxative Plus Stool Softener | DOCUSATE SODIUM 50 MG AND SENNOSIDES 8.6 MG | Preferred Pharmaceuticals, Inc. | b25b8a28-5e00-4a20-9ca3-7ed494fc4540 | 2026-09-01 | Warnings | F05Q2T2JA0 |
| Sulfamethoxazole and Trimethoprim | SULFAMETHOXAZOLE AND TRIMETHOPRIM | ATLANTIC BIOLOGICALS CORP. | acc3df02-1e99-46e6-8a31-9b26261c6daa | 2026-08-25 | Warnings, Adverse reactions | AN164J8Y0X JE42381TNV |
| HyVee Senna S | DOCUSATE SODIUM, SENNOSIDES | HyVee Inc | 4982b9c6-ed0e-24da-e063-6394a90a147f | 2026-08-24 | Warnings | F05Q2T2JA0 |
| Stool Softener Laxative | DOCUSATE SODIUM | Dolgencorp, Inc. (DOLLAR GENERAL & REXALL) | ccec364a-3135-4a5d-b4b0-86b832387b4e | 2026-08-24 | Warnings | F05Q2T2JA0 |
| Colace | DOCUSATE SODIUM | Atlantis Consumer Healthcare, Inc. | a1591da0-a1a9-9583-3cf5-788b8fee3814 | 2026-08-24 | F05Q2T2JA0 | |
| HyVee Senna S | DOCUSATE SODIUM, SENNOSIDES | HyVee Inc | 49837b2c-492f-2fed-e063-6294a90aaa24 | 2026-08-21 | Warnings | F05Q2T2JA0 |
| Senokot-S | STANDARDIZED SENNA CONCENTRATE AND DOCUSATE SODIUM | Atlantis Consumer Healthcare, Inc. | c24cdc5e-62e0-41a6-8afb-512202a569f4 | 2026-08-21 | Warnings | F05Q2T2JA0 |
| Foster and Thrive Senna-S Sennosides and Docusate Sodium Laxative and Stool Softener | DOCUSATE SODIUM 50MG AND SENNOSIDES 8.6MG | Strategic Sourcing Services LLC | 5966ff80-7be2-788a-e063-6294a90ab4f3 | 2026-08-19 | Warnings | F05Q2T2JA0 |
| Stool Softener Laxative | DOCUSATE SODIUM AND SENNOSIDES | Safeway, Inc. | ae2c7300-f9c4-43b5-9f8e-30f2e7d17635 | 2026-08-19 | Warnings | F05Q2T2JA0 |
| CVS Stool Softener Fruit Punch | DOCUSATE SODIUM | CVS PHARMACY, INC | 0e6900d6-7dc9-47d6-a006-1695feb8d5a5 | 2026-08-17 | Warnings | F05Q2T2JA0 |
| Stool Softener Laxative | DOCUSATE SODIUM | Dolgencorp, Inc. (DOLLAR GENERAL & REXALL) | 306fd12b-ed60-40dc-a5be-2dc394bd29d2 | 2026-08-17 | Warnings | F05Q2T2JA0 |
| Docusate Sodium and Sennosides | DOCUSATE SODIUM AND SENNOSIDES | Morepen Bio Inc | 562d1b9a-09d8-92fc-e063-6394a90a1993 | 2026-08-14 | Warnings | F05Q2T2JA0 |
| Stool Softener | DOCUSATE SODIUM | Dolgencorp, Inc. (DOLLAR GENERAL & REXALL) | f4671579-aed0-4f93-ab83-248e0d72b5b0 | 2026-08-10 | Warnings | F05Q2T2JA0 |
| Sulfamethoxazole and Trimethoprim | SULFAMETHOXAZOLE AND TRIMETHOPRIM | REMEDYREPACK INC. | ce44959b-4bfe-4ba9-9fc2-7f9d4663d542 | 2026-08-10 | Warnings, Adverse reactions | ANDA090624 198334 AN164J8Y0X JE42381TNV |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.