NDC 51660-423 – Ibuprofen and Pseudoephedrine hydrochloride
Ibuprofen 200 mg/1; Pseudoephedrine Hydrochloride 30 mg/1 · Tablet, Sugar Coated · Oral
Product NDC51660-423
Product details
- Brand name
- Ibuprofen and Pseudoephedrine hydrochloride
- Generic name
- Ibuprofen and pseudoephedrine hydrochloride
- Labeler
- Ohm Laboratories Inc.
- Dosage form
- Tablet, Sugar Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA074567
- Marketed since
- October 13, 2001
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nonsteroidal Anti-inflammatory Drug; alpha-Adrenergic Agonist
Active ingredients
- Ibuprofen 200 mg/1
- Pseudoephedrine Hydrochloride 30 mg/1
Uses, dosage, side effects and warnings for Ibuprofen and Pseudoephedrine Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 51660-423-21 | 20 TABLET, SUGAR COATED in 1 BLISTER PACK (51660-423-21) | Oct 13, 2001 |
| 51660-423-41 | 40 TABLET, SUGAR COATED in 1 BLISTER PACK (51660-423-41) | Oct 13, 2001 |
Other Ibuprofen and Pseudoephedrine Hydrochloride products
- 56062-423 Ibuprofen 200 mg/1; Pseudoephedrine Hydrochloride 30 mg/1 · Tablet, Sugar Coated · Publix Super Markets Inc
- 62011-0070 Ibuprofen 200 mg/1; Pseudoephedrine Hydrochloride 30 mg/1 · Tablet, Sugar Coated · Strategic Sourcing Services LLC
- 58602-839 Ibuprofen 200 mg/1; Pseudoephedrine Hydrochloride 30 mg/1 · Tablet, Coated · Aurohealth LLC
- 11822-0084 Ibuprofen 200 mg/1; Pseudoephedrine Hydrochloride 30 mg/1 · Tablet, Coated · Rite-Aid