Phenobarbital
- Product NDC
- 0603-5167
- 11-digit product format
- 006035167
- Labeler code
- 0603
- Product ID
- 0603-5167_f8c5136e-e35c-4425-8d49-b7f92c827b42
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- phenobarbital
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Par Health USA, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2001-12-01
- Marketing end
- 2027-02-28
- Substance
- PHENOBARBITAL
- Active strength
- 64.8 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Phenobarbital
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PHENOBARBITAL | 64.8 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | YQE403BP4D |
| Rxcui | 198086, 199164, 199167, 199168 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0603-5167-21 | Phenobarbital | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 13 |
| 0603-5167-32 | Phenobarbital | 1000 in 1 BOTTLE, PLASTIC | TABLET | 1000 | | 13 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0603-5167 | PHENOBARBITAL TABLET [ENDO USA, INC.] | 12 | Current NDC, Legacy NDC, 2 package rows | 20240913_069b92ce-0061-4724-8c25-08d8596770a2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0603-5167-21 | 00603516721 | 100 TABLET in 1 BOTTLE, PLASTIC (0603-5167-21) | 100 tablet | 2001-12-01 | 2027-02-28 | No | No | Current |
| 0603-5167-32 | 00603516732 | 1000 TABLET in 1 BOTTLE, PLASTIC (0603-5167-32) | 1000 tablet | 2001-12-01 | 2026-05-31 | No | No | Current |