Acetaminophen tablets USP 500 mg (Round)
- Manufacturer
- Granules India Limited
- Effective date
- 2023-01-27
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-05-31 23:54:02
Label at a glance#
ProductAcetaminophen 500 mg Round
Active ingredientACETAMINOPHEN
Label structure1 sections
Label contents#
Full prescribing information#
DailyMed RxNorm Mappings#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 62207-538-85 | Acetaminophen 500 mgRound | 90000 in 1 BOX | TABLET | 90000 | 3 | |
| 62207-538-87 | Acetaminophen 500 mgRound | 15000 in 1 BOX | TABLET | 15000 | 3 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Acetaminophen 500 mg Round
- Acetaminophen
- POLYETHYLENE GLYCOL, UNSPECIFIED
- STEARIC ACID
- LECITHIN, SOYBEAN
- FD&C RED NO. 40
- POVIDONE K30
- FD&C YELLOW NO. 6
- STARCH, CORN
- SUCRALOSE
- TALC
- TITANIUM DIOXIDE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 62207-538 | 62207-538-87, 62207-538-85 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| POLYETHYLENE GLYCOL, UNSPECIFIED | 3WJQ0SDW1A | IACT |
| STEARIC ACID | 4ELV7Z65AP | IACT |
| LECITHIN, SOYBEAN | 1DI56QDM62 | IACT |
| FD&C RED NO. 40 | WZB9127XOA | IACT |
| POVIDONE K30 | U725QWY32X | IACT |
| FD&C YELLOW NO. 6 | H77VEI93A8 | IACT |
| ACETAMINOPHEN | 362O9ITL9D | ACTIB |
| STARCH, CORN | O8232NY3SJ | IACT |
| SUCRALOSE | 96K6UQ3ZD4 | IACT |
| TALC | 7SEV7J4R1U | IACT |
| TITANIUM DIOXIDE | 15FIX9V2JP | IACT |
Source Document#
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 |
|---|---|---|---|---|---|---|
| f339915b-70e9-3ab6-e053-2a95a90a1b91 | ebe97ec1-bb02-9dc4-e053-2995a90a149d | 2023-01-27 | f339915b-70e9-3ab6-e053-2a95a90a1b91 ebe97ec1-bb02-9dc4-e053-2995a90a149d |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
