Acetaminophen Tablets USP 500 mg (Caplet)
- Manufacturer
- Granules India Limited | GRANULES LIFE SCIENCES PRIVATE LIMITED
- Effective date
- 2026-10-07
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 9
- Source
- daily-update
- Hydrated at
- 2026-10-10 01:02:51
Label at a glance#
ProductAcetaminophen Caplet
Active ingredientACETAMINOPHEN
Label structure1 sections
Label contents#
Full prescribing information#
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Data code | Code 128 | (00)189038320000000004 | 62207-177-85.jpg |
Products#
Every source-derived product name is available through these pages.
- Acetaminophen Caplet
- Acetaminophen
- POLYETHYLENE GLYCOL, UNSPECIFIED
- STEARIC ACID
- SODIUM STARCH GLYCOLATE TYPE A POTATO
- STARCH, CORN
- POVIDONE K30
- HYPROMELLOSE, UNSPECIFIED
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 62207-177 | 62207-177-81, 62207-177-85 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ACETAMINOPHEN | 362O9ITL9D | ACTIB |
| POLYETHYLENE GLYCOL, UNSPECIFIED | 3WJQ0SDW1A | IACT |
| STEARIC ACID | 4ELV7Z65AP | IACT |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | 5856J3G2A2 | IACT |
| STARCH, CORN | O8232NY3SJ | IACT |
| POVIDONE K30 | U725QWY32X | IACT |
| HYPROMELLOSE, UNSPECIFIED | 3NXW29V3WO | IACT |
Source Document#
Older Hydrated Versions#
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 8 | 2025-10-16 | full-release | 2026-06-01 01:39:21 |
| 7 | 2024-02-22 | full-release | 2026-06-01 00:08:57 |
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 |
|---|---|---|---|---|---|---|
| 414548cd-1e67-91da-e063-6294a90a3646 | 6176f9a2-6f2a-dcf6-e053-2a91aa0aee34 | 2025-10-16 | 6176f9a2-6f2a-dcf6-e053-2a91aa0aee34 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.


