Chloroquine
- Product NDC
- 0143-1195
- 11-digit product format
- 001431195
- Labeler code
- 0143
- Product ID
- 0143-1195_6c3b6cb9-0270-4ce5-aa51-fc8834f39880
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chloroquine Phosphate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- West-ward Pharmaceutical Corp
- Application
- ANDA083082
- Marketing category
- ANDA
- Marketing start
- 1975-07-09
- Marketing end
- 0000-00-00
- Substance
- CHLOROQUINE PHOSPHATE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Antimalarial [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status.
Orange Book products#
Application-product, Trade name, Ingredient table| Application-product | Trade name | Ingredient | Strength | Dosage form / route | TE codes | RLD / RS | Approval date |
|---|
| A083082-001 | CHLOROQUINE PHOSPHATE | CHLOROQUINE PHOSPHATE | 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | | Approved before 1982 | |
| A083082-002 | CHLOROQUINE PHOSPHATE | CHLOROQUINE PHOSPHATE | 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | | | 1999-09-17 |