PROMETHAZINE HYDROCHLORIDE
- Product NDC
- 63629-7670
- 11-digit product format
- 636297670
- Labeler code
- 63629
- Product ID
- 63629-7670_769495dc-102a-471e-b460-57556c26286d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- promethazine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040712
- Marketing category
- ANDA
- Marketing start
- 2006-07-31
- Marketing end
- 0000-00-00
- Substance
- PROMETHAZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7670-1 | 63629767001 | 6 TABLET in 1 BOTTLE (63629-7670-1) | 6 tablet | 2007-08-10 | 0000-00-00 | No | No | Current |
| 63629-7670-2 | 63629767002 | 10 TABLET in 1 BOTTLE (63629-7670-2) | 10 tablet | 2007-08-10 | 0000-00-00 | No | No | Current |
| 63629-7670-3 | 63629767003 | 12 TABLET in 1 BOTTLE (63629-7670-3) | 12 tablet | 2007-08-10 | 0000-00-00 | No | No | Current |