Obsidian
- Product NDC
- 63083-8135
- 11-digit product format
- 630838135
- Labeler code
- 63083
- Product ID
- 63083-8135_24ebbd96-2b39-40fa-bf39-49c6039c53de
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Obsidian
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Professional Complementary Health Formulas
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1984-08-15
- Marketing end
- 0000-00-00
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 6 [hp_X]/59mL
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63083-8135 | OBSIDIAN 8135 (OBSIDIAN) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] | 1 | Legacy NDC | 20220218_684ce0de-33c3-4f84-8cfc-42a7f49137e5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63083-8135-2 | 63083813502 | 59 mL in 1 BOTTLE, DROPPER (63083-8135-2) | 59 ml | 1985-08-15 | 0000-00-00 | No | No | Current |