Sinus and Headache
- Product NDC
- 79903-155
- Requested package NDC
- 79903-155-48
- 11-digit product format
- 799030155
- Labeler code
- 79903
- Product ID
- 79903-155_a1ded584-c24d-48bb-8d13-797c6d29c9fd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Phenylephrine HCl
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- WALMART INC.
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2005-07-26
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 325 mg/1; mg/1
- Pharmacologic classes
- Adrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- 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 package | package | 79903-155 | 79903-155-48 | D | Discontinued by firm | 2026-10-15 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 79903-155-48 | 79903015548 | 4 BLISTER PACK in 1 CARTON (79903-155-48) > 12 TABLET, FILM COATED in 1 BLISTER PACK | 4 blister pack | 2005-07-26 | 0000-00-00 | No | No | Current |