Ibuprofen and Diphenhydramine HCl
- Product NDC
- 59726-165
- 11-digit product format
- 597260165
- Labeler code
- 59726
- Product ID
- 59726-165_3a640ae7-ef01-469b-8454-c6225d240cd3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- IBUPROFEN, DIPHENHYDRAMINE HCL
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- P & L Development, LLC
- Application
- ANDA090397
- Marketing category
- ANDA
- Marketing start
- 2011-09-01
- Marketing end
- 2019-12-31
- 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