Chlorpromazine hydrochloride
- Product NDC
- 16714-049
- 11-digit product format
- 167140049
- Labeler code
- 16714
- Product ID
- 16714-049_13fe8f97-37e8-4d10-87fe-e1d17f4f23d8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorpromazine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Northstar Rx LLC
- Application
- ANDA213368
- Marketing category
- ANDA
- Marketing start
- 2020-05-11
- Substance
- CHLORPROMAZINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Chlorpromazine hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CHLORPROMAZINE HYDROCHLORIDE | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9WP59609J6 |
| Rxcui | 991039, 991044, 991188, 991194, 991336 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 16714-049-01 | Chlorpromazine hydrochloride | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 16714-049 | CHLORPROMAZINE HYDROCHLORIDE TABLET, FILM COATED [NORTHSTAR RX LLC] | 4 | Current NDC, Legacy NDC, 1 package rows | 20240814_2bd42d3a-bf89-4d74-a252-9b914106a570.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16714-049-01 | 16714004901 | 100 TABLET, FILM COATED in 1 BOTTLE (16714-049-01) | 2020-05-11 | 0000-00-00 | No | No | Current |