Acetaminophen, Phenylephrine Hydrochloride
- Product NDC
- 57344-123
- 11-digit product format
- 573440123
- Labeler code
- 57344
- Product ID
- 57344-123_d15617fb-6e32-f136-e053-2995a90ada1a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- AAA Pharmaceutical, Inc.
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2012-04-30
- Marketing end
- 2022-06-30
- Substance
- ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 325 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 57344-123-05 | 57344012305 | 2 BLISTER PACK in 1 CARTON (57344-123-05) > 12 TABLET, COATED in 1 BLISTER PACK | 2 blister pack | 2012-04-30 | 0000-00-00 | No | No | Current |