Promethazine Hydrochloride and Codeine Phosphate
- Product NDC
- 17856-0804
- 11-digit product format
- 178560804
- Labeler code
- 17856
- Product ID
- 17856-0804_bac94880-a702-43e3-ba7e-0c62928a0c31
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Promethazine Hydrochloride and Codeine Phosphate
- Dosage form
- SYRUP
- Route
- ORAL
- Labeler
- Atlantic Biologicals Corps
- Application
- ANDA040151
- Marketing category
- ANDA
- Marketing start
- 1997-08-26
- Marketing end
- 0000-00-00
- Substance
- PROMETHAZINE HYDROCHLORIDE; CODEINE PHOSPHATE
- Active strength
- 6 mg/5mL; mg/5mL
- Pharmacologic classes
- Phenothiazine [EPC],Phenothiazines [CS],Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CV
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
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FDA-Initiated Inactive NDC Indexing#
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