Phenylephrine Hydrochloride
- Product NDC
- 50090-4515
- 11-digit product format
- 500904515
- Labeler code
- 50090
- Product ID
- 50090-4515_a30c2d5c-89c0-4ea0-918f-a2b49f071362
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenylephrine Hydrochloride
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- A-S Medication Solutions
- Application
- NDA207926
- Marketing category
- NDA
- Marketing start
- 2015-01-15
- Marketing end
- 0000-00-00
- Substance
- PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 25 mg/mL
- Pharmacologic classes
- alpha-1 Adrenergic Agonist [EPC],Adrenergic alpha1-Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4515-1 | 50090451501 | 1 BOTTLE, DROPPER in 1 CARTON (50090-4515-1) > 15 mL in 1 BOTTLE, DROPPER | 2019-09-10 | 0000-00-00 | No | No | Current |