ZANG QI
- Product NDC
- 51673-001
- 11-digit product format
- 516730001
- Labeler code
- 51673
- Product ID
- 51673-001_93eef5c7-3b70-4633-b4ed-c5ba1aafe228
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- CAMPHOR (NATURAL)
- Dosage form
- PLASTER
- Route
- TRANSDERMAL
- Labeler
- QINGHAI ZANGYUANTANG BIO-TECH CO LTD
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2010-06-04
- Marketing end
- 0000-00-00
- Substance
- CAMPHOR (NATURAL)
- Active strength
- 3 g/1
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51673-001-01 | ZANG QI | 5 in 1 BOX | PLASTER | 5 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51673-001 | ZANG QI (CAMPHOR (NATURAL)) PLASTER [QINGHAI ZANGYUANTANG BIO-TECH CO LTD] | 1 | Legacy NDC, 1 package rows | 20100609_0fbb7035-0f36-46d2-bf7a-b13e4051e9ec.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 51673-001-01 | 51673000101 | 5 in 1 BOX | Historical |