Ibuprofen and Diphenhydramine HCl
- Product NDC
- 49035-858
- 11-digit product format
- 490350858
- Labeler code
- 49035
- Product ID
- 49035-858_0f485898-4845-46ca-be51-a289dd648a73
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- IBUPROFEN, DIPHENHYDRAMINE HCL
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- EQUATE (Wal-Mart Stores, Inc.)
- Application
- ANDA200888
- Marketing category
- ANDA
- Marketing start
- 2018-04-30
- Marketing end
- 2024-04-26
- Substance
- IBUPROFEN; DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 200 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49035-858-40 | 49035085840 | 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (49035-858-40) | 2018-04-30 | 2024-04-26 | No | No | Current |