Aspica (Aspirin)
- Product NDC
- 49638-101
- 11-digit product format
- 496380101
- Labeler code
- 49638
- Product ID
- 49638-101_5e87c71c-c05a-4333-a63d-ff20f85cc3d6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aspirin
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- America Medic & Science, LLC
- Application
- part343
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2020-07-06
- Marketing end
- 0000-00-00
- Substance
- ASPIRIN
- Active strength
- 81 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 49638-101 | I | Inactivated by FDA | 2026-10-05 | ||
| excluded package | package | 49638-101 | 49638-101-12 | I | Inactivated by FDA | 2026-10-05 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| d7724692-1155-4cc8-a415-22f5fc4aec35 | Product name | 6 | 20220216 |
| bde672ba-4805-28d0-1986-73543d41b412 | Product name | 2 | 20210201 |
| f212291f-05fe-9603-fc7e-bd73e38ce1e6 | Product name | 2 | 20161129 |
| ade821ba-260a-47e2-bd89-743e27ac9906 | Product name | 1 | 20161121 |
| 182f9ab4-4ab5-c449-200f-87ce2ce8e550 | Product name | 2 | 20151105 |
| 9425d234-4ae1-4b53-adc6-8cc7af6dd657 | Product name | 1 | 20150929 |
| 2a21311a-89e2-0e83-2ebd-117f9798b2b2 | Product name | 1 | 20140508 |
| 9007e8a7-ff50-f9b9-7945-f2a1deadd94e | Product name | 1 | 20140508 |
| 96c2be53-8e44-452d-56a2-d255b2f1af2d | Product name | 1 | 20140508 |
| bf8bd5f7-495f-4022-2780-7ded7ea7ea44 | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 49638-101-12 | 2024-01-11 | C162847 | 48780-1 | f386c64a-3487-0266-e053-dadaa90a7c1a | 9ca411d6-bfaf-4ed3-ae01-c30520aa5bbd |
| 49638-101-12 | 2023-01-30 | C162847 | 48780-1 | f386c64a-3487-0266-e053-dadaa90a7c1a | 9ca411d6-bfaf-4ed3-ae01-c30520aa5bbd |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 49638-101-12 | Aspica (Aspirin) | 120 in 1 BOTTLE | TABLET, DELAYED RELEASE | 120 | 4 | |
| 49638-101-12 | Aspica (Aspirin) | 1 in 1 CARTON | TABLET, DELAYED RELEASE | 1 | 4 |
DailyMed Dashboard NDC Coverage#
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 308416 | aspirin 81 MG Delayed Release Oral Tablet | PSN | 9ca411d6-bfaf-4ed3-ae01-c30520aa5bbd | 4 |
| 308416 | aspirin 81 MG Delayed Release Oral Tablet | SCD | 9ca411d6-bfaf-4ed3-ae01-c30520aa5bbd | 4 |
| 308416 | ASA 81 MG Delayed Release Oral Tablet | SY | 9ca411d6-bfaf-4ed3-ae01-c30520aa5bbd | 4 |
| 308416 | aspirin 81 MG Enteric Coated Oral Tablet | SY | 9ca411d6-bfaf-4ed3-ae01-c30520aa5bbd | 4 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 49638-101-12 | 49638010112 | 1 BOTTLE in 1 CARTON (49638-101-12) > 120 TABLET, DELAYED RELEASE in 1 BOTTLE | 1 bottle | 2020-07-06 | 0000-00-00 | No | No | Current |